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• W4285809662 abstract "The human genome contains more than one million tandem repeats (TRs), DNA sequences containing multiple approximate copies of a motif repeated contiguously. TRs account for significant genetic variation, with 50 + diseases attributed to changes in motif number. A few diseases have been to be caused by small indels in variable number tandem repeats (VNTRs) including poly-cystic kidney disease type 1 (MCKD1) and monogenic type 1 diabetes. However, small indels in VNTRs are largely unexplored mainly due to the long and complex structure of VNTRs with multiple motifs. We developed a method, code-adVNTR, that utilizes multi-motif hidden Markov models to detect both, motif count variation and small indels, within VNTRs. In simulated data, code-adVNTR outperformed GATK-HaplotypeCaller in calling small indels within large VNTRs. We used code-adVNTR to characterize coding VNTRs in the 1000 genomes data identifying many population-specific variants, and to reliably call MUC1 mutations for MCKD1." @default.
• W4285809662 created "2022-07-19" @default.
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• W4285809662 date "2022-08-01" @default.
• W4285809662 modified "2023-10-16" @default.
• W4285809662 title "Detecting tandem repeat variants in coding regions using code-adVNTR" @default.
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• W4285809662 doi "https://doi.org/10.1016/j.isci.2022.104785" @default.
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