VARIANT DETECTION OF SEQUENCING ASSAYS
Methods for improving variant protection are provided. The methods include the steps of generating an in silico genome map that includes a primary path, and a secondary path comprising variants that were missed or incorrectly called in a sequence assembly simulation, aligning the secondary path to the primary path, convoluting the second path to the primary path, and identifying the variants based upon reads that align with the secondary path but not the primary path. All of method steps can be carried out using a computer. Systems incorporated these methods are also included.
1 . A method for improving variant detection, the method comprising:
generating an in silico genome map comprising:
a primary path; and
a secondary path comprising variants that were missed or incorrectly called in a sequence assembly simulation;
aligning the secondary path to the primary path;
convoluting the second path to the primary path; and
identifying the variants based upon reads that align with the secondary path but not the primary path.
2 . The method of claim 1 , wherein the aligning step comprises assembling the plurality of sequence reads to produce a contig.
3 . The method of claim 2 , wherein the aligning step further comprises aligning the contig to either the primary path or the secondary path of the graph genome.
4 . The method of claim 3 , wherein the aligning step further comprises aligning one or more of the plurality of sequence reads to the contig.
5 . The method of claim 1 , wherein the computer is operable to report the one or more variants from the plurality of sequence reads.
6 . A method for improving variant detection of a genetic test, the method comprising:
generating an in silico genome map:
a primary path; and
a secondary path comprising variants that were missed or incorrectly called in a sequence assembly simulation;
analyzing, using the computer, a plurality of sequence reads generated by sequencing nucleic acid from a sample to determine whether the test is able to identify the variants based on the alignment of the reads to the in silico genome map.
7 . The method of claim 6 , wherein the analyzing step comprises aligning, using the computer, a plurality of sequence reads to the genome map in a manner that allows the plurality of sequence reads to align to either the primary or secondary paths.
8 . The method of claim 7 , wherein the analyzing step further comprises convoluting, using the computer, sequence reads that align to the secondary path or the primary path.
9 . The method of claim 8 , wherein analyzing step further comprises identifying, using the computer, one or more variants from the plurality of sequence reads.