U.S. patent application number 11/899199 was filed with the patent office on 2008-04-03 for computer algorithm for automatic allele determination from fluorometer genotyping device.
This patent application is currently assigned to Applera Corporation. Invention is credited to Stephen Glanowski, Jeremy Heil, Ivy A. McMullen, Emily S. Winn-Deen.
Application Number | 20080082273 11/899199 |
Document ID | / |
Family ID | 27787477 |
Filed Date | 2008-04-03 |
United States Patent
Application |
20080082273 |
Kind Code |
A1 |
Glanowski; Stephen ; et
al. |
April 3, 2008 |
Computer algorithm for automatic allele determination from
fluorometer genotyping device
Abstract
The present invention provides methods and systems for an
automated method of identifying allele values from data files
derived from processed fluorophore emissions detected during the
observation of fluorophore labeled nucleotide probes used in
analyzing polymorphic DNA are provided. These methods are used in
the rapid and efficient distinguishing of targeted polymorphic DNA
sites without control samples.
Inventors: |
Glanowski; Stephen; (Great
Falls, MD) ; Heil; Jeremy; (Derwood, MD) ;
Winn-Deen; Emily S.; (Potomac, MD) ; McMullen; Ivy
A.; (Towson, MD) |
Correspondence
Address: |
KILYK & BOWERSOX, P.L.L.C.
3603 CHAIN BRIDGE ROAD
SUITE E
FAIRFAX
VA
22030
US
|
Assignee: |
Applera Corporation
Foster City
CA
|
Family ID: |
27787477 |
Appl. No.: |
11/899199 |
Filed: |
September 5, 2007 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
|
10085142 |
Mar 1, 2002 |
7272506 |
|
|
11899199 |
Sep 5, 2007 |
|
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Current U.S.
Class: |
702/20 |
Current CPC
Class: |
G16B 40/00 20190201;
G16B 20/00 20190201; G06F 16/285 20190101 |
Class at
Publication: |
702/020 |
International
Class: |
G01N 33/48 20060101
G01N033/48 |
Claims
1. A method for categorizing a dataset comprising a plurality of
datapoints, each datapoint comprising at least two numerical
values, said method comprising the steps of: (a) producing a
plurality of angular values by calculating an angular value for
each datapoint based on said datapoint's numerical values; (b)
sorting said plurality of datapoints by said angular values; (c)
producing a plurality of difference values by calculating
differences between adjacent angular values; (d) determining at
least one category-dividing value by identifying at least one
difference value above a predetermined threshold gap value; and (e)
classifying at least one datapoint according to its angular value
relative to at least one category-dividing value.
2. The method of claim 1 wherein each datapoint comprises two
numerical values.
3. The method of claim 2 wherein said angular value is an
arctangent of said two numerical values.
4. The method of claim 1 wherein said numerical values represent
fluorometric data.
5. The method of claim 1 wherein said determining step (d)
identifies two category-dividing values.
6. The method of claim 1 further comprising the step of normalizing
said numerical values to a scale.
7. The method of claim 6 wherein said scale ranges from 0.0 to
1.0.
8. The method of claim 1 further comprising the step of removing
non-amplification datapoints from said dataset, said step
comprising the steps of: (i) calculating a Euclidean distance for
each datapoint; (ii) removing at least one datapoint from said
dataset, wherein the Euclidean distance of said datapoint falls
below a predetermined distance threshold.
9. The method of claim 1 wherein said determining step (d)
identifies two category-dividing values comprising a first and a
second category-dividing value, and said classifying step (e)
comprises the steps of: (i) classifying at least one datapoint in a
first category, wherein all datapoints of said first category have
an angular value lower than said first and second category-dividing
values; (ii) classifying at least one datapoint in a second
category, wherein all datapoints of said second category have an
angular value between said first and second category-dividing
values; and (iii) classifying at least one datapoint in a third
category, wherein all datapoints of said third category have an
angular value greater than said first and second category-dividing
values.
10. The method of claim 9 wherein classification in said first
category corresponds to homozygosity for a first allele,
classification in said third category corresponds to homozygosity
for a second allele, and classification in said second category
corresponds to heterozygosity for said first and second
alleles.
11. The method of claim 10 further comprising the step of
determining the presence of a condition to bring to the attention
of a human user, wherein said condition comprises the proportion of
datapoints classified as heterozygous exceeding a predetermined
threshold.
12. The method of claim 11 further comprising the step of
determining the presence of a condition to bring to the attention
of a human user.
13. The method of claim 12 wherein said condition comprises a
substantial majority of datapoints being classified in one
category.
14. The method of claim 13 wherein said category corresponds to
heterozygosity for a first and second allele.
15. The method of claim 13 wherein said category corresponds to
homozygosity for either a first or second allele.
16. The method of claim 13 wherein said category cannot be
determined to correspond to either heterozygosity or
homozygosity.
17. The method of claim 12 wherein said condition comprises said
datapoints being classified into more than three categories.
18. The method of claim 12 wherein said condition comprises at
least one of said datapoints remaining unclassified.
19. The method of claim 12 wherein said condition comprises the
Euclidean distance between at least one of said classified
datapoints and at least one non-amplification datapoint being below
a predetermined threshold.
20. The method of claim 12 wherein said condition comprises a
substantial majority of datapoints in said first category having an
angular value higher than a predetermined threshold.
21. The method of claim 20 wherein said angular value is an
arctangent and said predetermined threshold is 0.67.
22. The method of claim 12 wherein said condition comprises a
substantial majority of datapoints in said third category having an
angular value lower than a predetermined threshold.
23. The method of claim 22 wherein said angular value is an
arctangent and said predetermined threshold is 1.0.
24. The method of claim 12 wherein said condition comprises a
substantial majority of datapoints in said second category having
an angular value lower than a first predetermined threshold or
higher than a second predetermined threshold.
25. The method of claim 24 wherein said angular value is an
arctangent, said first predetermined threshold is 0.18, and said
second predetermined threshold is 1.35.
26. The method of claim 12 wherein said condition comprises the
difference between the largest angular value of a datapoint in a
category and the smallest angular value of a datapoint in the
category exceeding a predetermined threshold.
27. The method of claim 26 wherein said angular value is an
arctangent and said second predetermined threshold is 0.6.
28. The method of claim 12 wherein said first allele is a major
allele and said second allele is a minor allele, and said major and
minor alleles are in a Hardy-Weinberg equilibrium.
29. The method of claim 28 further comprising the step of
determining the presence of a condition to bring to the attention
of a human user, wherein said condition indicates an
incompatibility with a Hardy-Weinberg equilibrium.
30. The method of claim 29 wherein said incompatibility comprises a
greater number of datapoints classified as homozygous for said
minor allele than classified as heterozygous.
31. The method of claim 12 further comprising the step of
determining the presence of a condition to bring to the attention
of a human user, said determining step comprising the steps of: (i)
calculating the center of the set of removed datapoints, said
center comprising an x and y coordinate; and (ii) determining if
either said x or y coordinate exceeds a predetermined
threshold.
32. The method of claim 31 wherein said predetermined threshold is
0.3 on a normalized scale of 0.0 to 1.0.
33. A method for performing allelic differentiation comprising:
acquiring fluorescence intensity data for a plurality of samples
wherein the fluorescence intensity data is obtained by
amplification of each sample in the presence of at least two
fluorophore labels; generating an angular value for each sample by
comparing the fluorescence intensity obtained for the at least tow
fluorophore labels; arranging the samples according to their
angular value to form an angular-valued based distribution of the
samples; determining a difference value for each sample by taking
the difference between the angular value for a selected sample and
the angular value for an adjacent sample; associating at least one
difference value range with a selected allelic composition;
evaluating each sample's difference value with respect to the at
least one difference value range to determine if the sample resides
within the range; and identifying the allelic composition of each
sample on the basis of the difference value range which the sample
resides within.
34. The method of claim 33, wherein the allelic compositions
comprises a homozygous allele.
35. The method of claim 33, wherein the allelic compositions
comprises a heterozygous allele.
36. The method of claim 33, wherein the angular values for each
sample are normalized.
37. The method of claim 33, wherein the angular values are
calculated as the arctangent between the at least two fluorophore
labels.
38. The method of claim 33, further comprising reducing the number
of samples undergoing analysis by: calculating a Euclidean distance
for each sample; and identifying a Euclidean distance threshold for
which samples having a Euclidean distance below the threshold are
removed from further analysis.
39. A method for genotypic analysis comprising: amplifying a
plurality of a genetic samples in the presence of at least two
discriminable labels to thereby obtain intensity information
indicative of the signals generated by the at least tow
discriminable labels during amplification; calculating an angular
value for each sample by comparing the intensity information for
the at least two discriminable labels used during amplification;
ordering the samples on the basis of their angular value;
calculating a difference value for each sample by taking the
difference between the angular value for a selected sample and the
angular value for an adjacent sample; identifying difference value
ranges corresponding to homozygous and heterozygous allelic
variations; and determining whether a sample corresponds to a
homozygous or heterozygous allelic variant by determining if the
sample's difference value resides within the difference value
ranges corresponding to homozygous or heterozygous allelic
variation.
40. The method of claim 39, wherein the angular values for each
sample normalized prior to difference value determination.
41. The method of claim 39, wherein the angular values are
calculated as the arctangent between the at least two discriminable
labels.
42. The method of claim 41, further comprising identifying at least
one of the discriminable labels as undetermined based on at least
one predetermined condition.
43. The method of claim 42, wherein the at least one predetermined
condition is based on comparison of the dye emissions to a control
probe.
44. The method of claim 43, wherein the at least one predetermined
condition is based on a range between a maximum and minimum
fluorescence dye emission.
45. A method for genotypic analysis comprising: receiving intensity
information for a plurality of samples comprising intensity data of
at least first and second fluorescent probes; calculating a range
between a maximum and minimum of the emission data for each of the
first and second fluorescent probes; determining whether the range
between the maximum and minimum of the emission data for each of
the at least first and second fluorescent probes exceeds a
predetermined threshold; determining whether a plurality of
clusters of datapoints defined by emission data of the at least
first and second fluorescent probes is present based on whether the
range between the maximum and minimum of the emission data exceeds
the predetermined threshold for each of the at least first and
second fluorescent probes; and, when a plurality of clusters are
present calculating an angular value for each sample of the
plurality of sample by comparing the intensity information for the
at least first and second fluorescent, ordering the plurality of
samples on the basis of their angular value, calculating a
difference value for each sample by taking the difference between
the angular value for a selected sample and the angular value for
an adjacent sample, identifying difference value ranges
corresponding to homozygous and heterozygous allelic variations,
and determining whether a sample corresponds to a homozygous or
heterozygous allelic variant by determining if the sample's
difference value resides within the difference value ranges
corresponding to homozygous or heterozygous allelic variation.
Description
[0001] This application is a continuation application of U.S.
patent application Ser. No. 10/085,142, filed Mar. 1, 2002, which
is incorporated herein in its entirety by reference.
FIELD OF THE INVENTION
[0002] The invention relates generally to the field of DNA
genotypic analysis. More particularly, the invention relates to the
allelic classification of DNA samples through cluster analysis of
analyzed emission spectra observed from excited fluorophore-labeled
nucleotide probes. Specifically, fluorophore-labeled nucleotide
probes can be used verify DNA variations between individual samples
and verify the expression of a region of DNA in different cell
lines.
BACKGROUND OF THE INVENTION
[0003] Individual DNA sequence variations are known to directly
cause specific diseases or conditions, or to predispose certain
individuals to specific diseases or conditions. Such variations
also modulate the severity or progression of many diseases.
Additionally, DNA sequence variations exist between populations.
Therefore, determining DNA sequence variations is useful for making
accurate diagnoses, for finding suitable therapies, and for
understanding the relationship between genome variations and
environmental factors in the pathogenesis of diseases and
prevalence of conditions.
[0004] There are several types of DNA sequence variations. These
variations include insertions, deletions, restriction fragment
length polymorphisms ("RFLPs"), short tandem repeat polymorphisms
("STRPs"), and single nucleotide polymorphisms ("SNPs"). Of these,
SNPs are considered the most useful in studying the relationship
between DNA sequence variations and diseases and conditions because
they are more common, more stable, and more amenable to being
employed in large-scale studies than other sorts of variations.
[0005] Currently, a set of over 3 million putative SNPs has been
identified in the human genome. It is a current goal of researchers
to verify these putative SNPs and associate them with phenotypes
and diseases, eventually replacing currently-used RFLP and STRP
linkage analysis screening sets. In order to successfully
accomplish this goal, it will be necessary for researchers to
generate and analyze large amounts of genotypic data.
[0006] A number of methods have been developed which can locate or
identify SNPs. These methods include dideoxy fingerprinting (ddF),
fluorescently labeled ddF, denaturation fingerprinting (in F1R and
DnF2R), single-stranded conformation polymorphism analysis,
denaturing gradient gel electrophoresis, heteroduplex analysis,
RNase cleavage, chemical cleavage, hybridization sequencing using
arrays and direct DNA sequencing.
[0007] One method of particular relevance to the present invention
employs a pair of fluorescent probes, each probe containing a
different dye and specific for a different allele. In this method,
the two probes are added to the DNA sample to be tested, and the
mixture is amplified using PCR. If the DNA sample is homozygous for
the first allele, the first probe's dye will exhibit a high degree
of fluorescence and the fluorescence from the second probe's dye
will be absent. Conversely, if the DNA sample is homozygous for the
second allele, the second probe's dye will exhibit a high degree of
fluorescence and the fluorescence from the first probe's dye will
be absent. If the DNA sample is heterozygous for both alleles, then
both probes should fluoresce equally. A commercial implementation
of this method is APPLIED BIOSYSTEMS' TAQMAN platform, which
employs APPLIED BIOSYSTEMS' PRISM 7700 and 7900HT SEQUENCE
DETECTION SYSTEMS to record the fluorescence of each sample's PCR
product.
[0008] A typical implementation generates amplification products
from a set of a large number of samples at a time, and measures a
pair of fluorescence values, one for each dye, from each amplified
sample. To classify the samples, it is useful to first plot the
fluorescence values of the entire set on a two dimensional graph,
and observe that the plotted points tend to cluster into separate
groups according to genotype, as illustrated in FIG. 1. In this
figure, a human observer can readily discern that the data falls
into four groups. The first group, in the lower-left hand corner,
represents samples that had no amplification or were a no template
control ("NTC") reaction. The second group, in the lower right hand
corner, represents those samples homozygous for Allele 2. The third
group, at the top, represents those samples homozygous for Allele
1. Finally, the fourth group, located between the second and third
groups, represents the heterozygous samples. This classification is
illustrated further in FIG. 2. Although it is relatively easy for
human observer to analyze this type of data, it is necessary to
develop a fast, reliable, and unsupervised method of computational
analysis to produce the level of throughput necessary to analyze
the large amounts of genotypic data generated.
[0009] Previous methods of computational analysis have employed a
family of algorithms known as clustering algorithms. A typical
clustering algorithm receives raw unstructured data and processes
it to form groups of data elements that are similar to each other.
Clustering algorithms are well known in the field of computer
science, and are typically applied in data mining applications. In
a data mining application, clustering is used to identify
relationships in data collections not readily observable to an
expert user due to the volume of information.
[0010] A typical clustering algorithm examines the distance between
data elements to find a common centroid. The centroid is mean of
the value of the data elements belonging to a cluster. Clusters are
selected by the algorithm to minimize the distance between the
elements contained within it relative to the elements contained in
other clusters. Clustering algorithms belong to the greater class
of unsupervised machine learning algorithms. Other supervised
machine learning algorithms, including decision trees and neural
networks, were considered for application to analyzing output from
a fluorometric genotyping device. However, all machine learning
algorithms considered were determined to be insufficient to analyze
this type of data accurately. A thorough review of initial
collection of 80 human reviewed outputs revealed characteristics of
the data that would not allow standard machine learning algorithms
to work with a high degree of accuracy.
[0011] It is an object of this invention to provide a fast,
accurate, and unsupervised method of classifying genotypic samples
based on fluorometric data generated from them.
SUMMARY OF THE INVENTION
[0012] In one aspect, the invention relates to a method for
categorizing the members of a dataset into discrete categories. In
this aspect the dataset has a plurality of datapoints, and each
datapoint has at least two numerical values associated with it. In
this aspect, the method has the following steps: Assign each
datapoint an angular value based on that datapoint's numerical
values; sort the dataset by angular value; calculate the
differences between adjacent angular values in the sorted dataset;
determining category-dividing values by identifying differences
that are larger than a predetermined threshold; and classifying
datapoints according to their angular values relative to the
category-dividing values.
[0013] In a further aspect, each datapoint has exactly two
numerical values, and the angular value is an arctangent of the
datapoint's numerical values. In a further aspect the numerical
values are normalized before the angular values are calculated.
[0014] In a further aspect, the numerical values represent
fluorometric data, wherein the different numerical values for each
datapoint represent the fluorescence of a different dye.
[0015] In a further aspect, the method identifies exactly two
category-dividing values and three categories. In a further aspect,
these three categories represent homozygosity for a first allele,
homozygosity for a second allele, and heterozygosity for both
alleles.
[0016] In a further aspect the fluorometric data is measured from
the product of an amplification reaction, and the method includes a
step for removing datapoints that represent either a control
reaction or a failure to amplify. In this aspect, the datapoints
whose Euclidean distance falls beneath a predetermined threshold
are removed from any further classification.
[0017] In a further aspect, the results of the classification are
examined to determine whether to bring them to the attention of a
human user. In this aspect, the results are examined for conditions
that indicate that the classification was unsuccessful. Such
conditions include excess classification in one category,
classification into more than three categories, absence or near
absence of any classification in one or more categories,
unclassified datapoints, inadequate separation from control or
nonamplification reactions, clusters having angular values that are
either too high or too low, clusters whose ranges of angular values
are too wide, classification that is not compatible with a
Hardy-Weinberg equilibrium, and control or nonamplification
reactions that are too far from the origin.
BRIEF DESCRIPTION OF THE DRAWINGS
[0018] FIG. 1 provides a two dimensional scatterplot of
fluorometric data.
[0019] FIG. 2 provides a two dimensional scatter plot of
fluorometric data classified by allele.
[0020] FIG. 3 provides a two dimensional scatterplot of raw
fluorometric data.
[0021] FIG. 4 provides a two dimensional scatterplot of normalized
fluorometric data.
[0022] FIG. 5 provides a two dimensional scatterplot of normalized
fluorometric data classified by allele.
[0023] FIG. 6 provides a two dimensional scatterplot of normalized
fluorometric data classified by allele, and undetermined datapoints
identified.
[0024] FIG. 7 provides a bargraph of the differences in arctangent
values between adjacent datapoints sorted by arctangent.
DETAILED DESCRIPTION OF INVENTION
[0025] Although the methods of the current invention can be used to
classify any kind of bivariate or multivariate data, they are
particularly useful for classifying genotypic data, especially
allelic data generated by fluorescence.
[0026] In one embodiment, the fluorometric genotyping device
generates for each sample a unique sample identifier, a value from
one of the sample's fluorometric probes, and a value from the
sample's other fluorometric probe. The paired fluorescence values
can then be plotted as x and y values on a two-dimensional grid.
Ideally, the data generated in this fashion should yield
heterozygous datapoints in the upper-right quadrant, and homozygous
datapoints for each allele in the upper-left and lower-right
quadrants, respectively. If that were the case, then allele calling
would be a simple matter of dividing the grid by quadrants.
However, fluorometric genotypic has been observed to exhibit
several characteristics and idiosyncrasies that must be addressed
in order for an automated allele caller to function accurately, and
have not been adequately addressed by previous methods of
clustering and machine learning.
[0027] Traditional machine learning algorithms such as decision
trees and neural networks generate solutions by training on a given
collection of data where the outcome is known and then applying the
trained system to predict data in unknown outcomes. Training these
algorithms with fluorometric data produces a solution where a set
of X and Y boundaries are defined that had the highest probability
of being correct. However, the predictions of results that deviate
from the trained form would have poor accuracy. Because
fluorometric data tends to vary from instance to instance, a
trained system is too rigid to be sufficiently accurate to operate
unsupervised on a large number of samples.
[0028] Another imperfection of fluorometric data is that outputs
from fluorometric genotyping devices can validly produce one to
three clusters, in addition to clusters formed by samples that had
no amplification or no template control reactions ("NTCs"). In
general, fluorometric genotyping devices are expected to produce
three clusters, but can validly produce only one or two. For
example, if three clusters are expected but only two valid clusters
are produced, then the datapoints could be invalidly categorized
into three clusters. Clustering algorithms are generally given a
fixed number of expected clusters, and any deviation from the
expected number of clusters greatly reduces their
effectiveness.
[0029] Another imperfection of fluorometric data is that datapoints
belonging to the same category can be spread out spatially. A
widely-spread cluster is usually observed for the category of
heterozygous genotypes, where both fluorometric probes are active.
A widely-spread cluster greatly reduces the effectiveness of
clustering algorithms, especially when the distance between the
furthest datapoints of a cluster and its centroid is greater than
their distance to other clusters. Furthermore, as noted above, the
number of valid clusters produced by fluorometric data can vary
from the expected three to one or two. For example if two valid
clusters are produced and one of them is widely-spread, it is
likely that a clustering algorithm will incorrectly divide that one
valid cluster into two invalid clusters.
[0030] In one embodiment, the dataset has a plurality of
datapoints, and each datapoint has two numerical values associated
with it. In an alternate embodiment, each datapoint has more than
two numerical values associated with it. In a further embodiment,
the numerical values represent quantitative empirical data. In yet
a further embodiment, the quantitative empirical data is measured
fluorescence. In a further embodiment, the numerical values are
normalized before being used in any subsequent calculations.
[0031] In this embodiment, an angular value is calculated for each
datapoint in the dataset based upon the datapoint's numerical
values. In a further embodiment, the angular value is an arctangent
of the numerical values. The dataset is then sorted by angular
value. A difference value is then calculated for each datapoint by
subtracting the angular value of the previous datapoint from that
of the current datapoint. The difference value of the first
datapoint is that point's angular value.
[0032] If the difference value is large enough to exceed a
predetermined threshold, a new category-dividing value is
designated between the two angle values from which that difference
value was calculated. In one embodiment, the category-dividing
value is the average of the two angle values from which the
above-threshold difference value was calculated. FIG. 7 illustrates
the difference values for an example dataset. In this example, the
samples are lined along the X-axis according to the rank of their
angular value, and each sample's difference value is plotted on the
Y-axis. As illustrated in FIG. 7, the results indicate the presence
of two difference values which stand out dramatically from the rest
of the data. Two dividing values are designated, one between sorted
samples 131 and 132 and the other between sorted samples 222 and
223, each at a angle value between the two angle values which
generated the above-threshold difference value.
[0033] As their name suggests, the category-dividing values are
subsequently used to separate datapoints into categories. In this
example, sorted datapoints 1-131 are classified as homozygous for a
first allele, sorted datapoints 132-222 are classified as
heterozygous, and samples 223-239 are classified as homozygous for
a second allele.
[0034] The data contained in the example illustrated in FIG. 7 and
described above are relatively clean and well-adapted to machine
analysis. In one embodiment, the data are examined for conditions
which indicate that the data are less well-formed and may not yield
correct results when subjected to unsupervised machine analysis. In
a further embodiment, if such conditions are detected, the method
adapts its analysis to the idiosyncrasies of the dataset in order
to yield a more accurate analysis. In yet a further embodiment, if
such conditions are detected the dataset is flagged to indicate
that it should be examined by a human reviewer.
[0035] In one embodiment, the data are examined to determine if
control samples are present in the dataset. In a further
embodiment, identified control samples are removed from the dataset
before any further classification is performed.
[0036] In one embodiment, the range between the maximum and minimum
observed values for each fluorophore-labeled nucleotide probe is
calculated. If the range falls below a predetermined threshold, it
is determined that the results are only valid for the other probe.
Those samples producing data with the valid probe are then
distinguished from samples that had no amplification or were NTCs.
In one embodiment, all datapoints within a predetermined distance
from the minimum observed values of the dataset are determined to
be NTCs and the remaining datapoints are classified as belonging to
the observed probe.
[0037] If, on the other hand, the range between maximum and minimum
observed values for each fluorophore-labeled nucleotide probe
exceeds the predetermined threshold, it is determined that multiple
clusters are probably present, and the following steps are taken:
All of the numerical values are normalized. In a further
embodiment, all of the numerical values are normalized on a scale
ranging from 0.0 to 1.0. Then the Euclidean distance between
minimum values and each sample is computed. Samples are predicted
as NTC or non-amplification and removed from further consideration
if their distance to minimum values fall below a predetermined
distance threshold.
[0038] The average distance of all remaining datapoints is then
computed and used to calculate a threshold. All remaining
datapoints that fall below this threshold are predicted as
undetermined and removed from further classification.
[0039] Once the above-described screening steps are performed, the
method of this embodiment proceeds similarly to that of the
previous example: Angular values are calculated for each datapoint;
the dataset is sorted by angular value; difference values are
calculated; category-dividing values are identified; and each
datapoint is categorized according to its angular value.
[0040] In one embodiment, the classification results are then
examined with a series of evaluations to determine if there are any
characteristics to bring to the attention of a human reviewer.
Examples of such conditions include excess classification in one
category, classification into more than three categories, absence
or near absence of any classification in one or more categories,
unclassified datapoints, inadequate separation from control or
nonamplification reactions, clusters having angular values that are
either too high or too low, clusters whose ranges of angular values
are too wide, classification that is not compatible with a
Hardy-Weinberg equilibrium, and control or nonamplification
reactions that are too far from the origin.
[0041] If the samples were identified as all homozygous, it not
considered an error of the clustering algorithm, but needs to be
noted to the investigator that the assay is not variable.
[0042] If only one cluster was identified and it could not be
determined to be all homozygous then the dataset is flagged to
indicate that human review is recommended.
[0043] If more than three clusters were identified then the dataset
is flagged so that a human user can review the calls.
[0044] If more than a preset number of datapoints are predicted as
undetermined then the dataset is flagged indicating that human
review is desired. In a further embodiment, this preset number is
4.
[0045] If the samples from a probe are not separated from the node
template controls by a threshold distance determined by the probe
technology used then the dataset is flagged to indicate that the
probe is producing a weak signal.
[0046] If the heterozygosity of the predicted calls is greater than
a given heterozygosity threshold then the dataset is flagged so
that a human user can review the predicted results. Heterozygosity
is the predicted number of heterozygous sample divided by the
number of heterozygous and homozygous samples.
[0047] If the homozygous cluster for a first allele is below an
arctangent of 1.0 then the dataset is flagged indicating that the
cluster is in too low of a position and should be human
reviewed.
[0048] If the homozygous cluster for a second allele is above an
arctangent of 0.67 then the database is flagged indicating that the
cluster is in too high of a position and should be human
reviewed.
[0049] If the heterozygous cluster is above an arctangent of 1.35
then the database is flagged indicating that the cluster is in too
high of a position and should be human reviewed. Similarly, if the
heterozygous cluster is below an arctangent of 0.18 then the
database is flagged indicating that the cluster is in too low of a
position and should be human reviewed.
[0050] If there are three clusters and the cluster with the
smallest number of samples, also known as the minor allele cluster,
is greater then the heterozygous cluster then these results do not
agree with population genetics Hardy-Weinberg principle and the
database is flagged so that a human will review the results.
[0051] If any cluster is wider then 0.6 from the start of the
cluster's arctangent to its end then the cluster is unusually wide
and the dataset is flagged to have the results human reviewed.
[0052] If the center of the predicted node template control cluster
is greater then 0.3 on a probe axis in a 0.0 to 1.0 normalized
coordinate system, this indicates a problem with the probe and the
dataset is flagged so the results are human reviewed.
EQUIVALENTS
[0053] The invention may be embodied in other specific forms
without departing from the spirit or essential characteristics
thereof. The foregoing embodiments are therefore to be considered
in all respects illustrative, rather than limiting, of the
invention described herein. Scope of the invention is thus
indicated by the appended claims, rather than by the foregoing
description, and all variants which fall within the meaning and
range of equivalency of the claims are therefore intended to be
embraced therein.
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