Determining the Clinical Significance of Variant Sequences

1 - 10 . (canceled)

11 . A method for determining a clinically significant variant sequence within a sequence read of a biological sample obtained from an organism, the method comprising:

sequencing, by a sequencer, nucleic acid to generate a plurality of sequence reads including the sequence read of the biological sample, wherein the nucleic acid was extracted from the biological sample, and at least the sequence read of the biological sample includes a sequence of nucleotide data less than about 150 bases in length;

receiving, by a computer included in or coupled to the sequencer, a reference sequence;

aligning, by the computer, at least the sequence read of the biological sample with the reference sequence;

identifying, by the computer, a variant sequence within the sequence read of the biological sample based on the aligning the sequence read with the reference sequence;

determining, by the computer and based on information from a variant database, that the identified variant sequence is a novel variant sequence not known to be disease-causing, wherein the variant database stores variant sequences associated with diseases;

generating, by the computer, an equivalent insertion or deletion region (EIR) of the variant sequence, the EIR comprising a region of nucleic acid representing equivalent positions of the variant sequence with respect to the reference sequence;

identifying, by the computer, a functional region that includes at least a portion of the EIR, wherein the functional region is described by gene structures and obtained by annotating the EIR of the variant sequence with protein coding region coordinates;

determining, by the computer, whether or not the EIR extends beyond the functional region; and

determining, by the computer, either that the variant sequence has clinical significance when the EIR does not extend beyond the functional region, or that the variant sequence does not have clinical significance when the EIR extends beyond the functional region.

12 . The method of claim 11 , wherein the variant sequence is determined to have clinical significance.

13 . The method of claim 11 , wherein the annotating the EIR of the variant sequence includes associating genomic coordinates of the variant sequence to the protein coding region coordinates.

14 . The method of claim 11 , wherein the gene structures include genes, exons, introns, splice sites, codons, or non-coding regions.

15 . The method of claim 11 , wherein the variant sequence is located in a tandem repeat.

16 . The method of claim 11 , wherein the variant sequence includes a splice site mutation, an in-frame mutation, a nonsense mutation, or a frameshift mutation.

17 . The method of claim 11 , wherein the biological sample includes haploid or diploid cells.

18 . A computer system, comprising:

a sequencer configured to sequence nucleic acid to generate a plurality of sequence reads, wherein the nucleic acid was extracted from a biological sample obtained from an organism, and at least a sequence read of the biological sample includes a sequence of nucleotide data less than about 150 bases in length;

a processor coupled to the sequencer, and configured to:

receive a reference sequence;

align at least the sequence read of the biological sample with the reference sequence;

identify a variant sequence within the sequence read based on the aligned sequence read with the reference sequence;

determine, based on information from a variant database, the identified variant sequence is a novel variant sequence that is not known to be disease-causing, wherein the variant database stores variant sequences associated with diseases;

generate an equivalent insertion or deletion region (EIR) of the variant sequence, the EIR comprising a region of nucleic acid representing equivalent positions of the variant sequence with respect to the reference sequence;

identify a functional region that includes at least a portion of the EIR, wherein the functional region is described by gene structures and obtained by annotating the EIR of the variant sequence with protein coding region coordinates;

determine whether or not the EIR extends beyond the functional region; and

determine, either that the variant sequence has clinical significance when the EIR does not extend beyond the functional region, or that the variant sequence does not have clinical significance when the EIR extends beyond the functional region.

19 . The computer system of claim 18 , wherein the variant sequence is determined to have clinical significance.

20 . The computer system of claim 18 , wherein the annotating the EIR of the variant sequence includes associating genomic coordinates of the variant sequence to the protein coding region coordinates.

21 . The computer system of claim 18 , wherein the gene structures include genes, exons, introns, splice sites, codons, or non-coding regions.

22 . The computer system of claim 18 , wherein the variant sequence is located in a tandem repeat.

23 . The computer system of claim 18 , wherein the variant sequence includes a splice site mutation, an in-frame mutation, a nonsense mutation, or a frameshift mutation.

24 . The computer system of claim 18 , wherein the biological sample includes haploid or diploid cells.

25 . A non-transitory computer-readable medium having instructions stored thereon that, when executed by at least one computing device, cause the at least one computing device to perform operations comprising:

receiving a plurality of sequence reads including a sequence read sequenced from a nucleic acid, wherein the nucleic acid was extracted from a biological sample obtained from an organism, and the sequence read includes a sequence of nucleotide data less than about 150 bases in length;

receiving a reference sequence;

aligning the sequence read with the reference sequence;

identifying a variant sequence within the sequence read based on the aligning the sequence read with the reference sequence;

determining, based on information from a variant database, whether the identified variant sequence is a novel variant sequence that is not known to be disease-causing, wherein the variant database includes variant sequences associated with diseases;

generating an equivalent insertion or deletion region (EIR) of the variant sequence, the EIR comprising a region of nucleic acid representing equivalent positions of the variant sequence with respect to the reference sequence;

identifying a functional region that includes at least a portion of the EIR, wherein the functional region is described by gene structures and obtained by annotating the EIR of the variant sequence with protein coding region coordinates;

determining whether or not the EIR extends beyond the functional region; and

determining either that the variant sequence has clinical significance when the EIR does not extend beyond the functional region, or that the variant sequence does not have clinical significance when the EIR extends beyond the functional region.

26 . The non-transitory computer-readable medium of claim 25 , wherein when the variant sequence is determined to have clinical significance.

27 . The non-transitory computer-readable medium of claim 25 , wherein the annotating the EIR of the variant sequence includes associating genomic coordinates of the variant sequence to the protein coding region coordinates.

28 . The non-transitory computer-readable medium of claim 25 , wherein the gene structures include genes, exons, introns, splice sites, codons, or non-coding regions.

29 . The non-transitory computer-readable medium of claim 25 , wherein the variant sequence is located in a tandem repeat.

30 . The non-transitory computer-readable medium of claim 25 , wherein the variant sequence includes a splice site mutation, an in-frame mutation, a nonsense mutation, or a frameshift mutation.