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Method

OMKar automates genome karyotyping using optical maps to identify constitutional abnormalities

  • First Published November 14, 2025
Method

CoRAL accurately resolves extrachromosomal DNA genome structures with long-read sequencing

  • First Published July 9, 2024
Method

Ancestry-agnostic estimation of DNA sample contamination from sequence reads

  • First Published January 24, 2020
Method

Targeted genotyping of variable number tandem repeats with adVNTR

  • First Published October 23, 2018
Method

HapCUT2: robust and accurate haplotype assembly for diverse sequencing technologies

  • First Published December 9, 2016
Method

An efficient and scalable analysis framework for variant extraction and refinement from population-scale DNA sequence data

  • First Published April 16, 2015
Method

Amplification and thrifty single-molecule sequencing of recurrent somatic structural variations

  • First Published December 4, 2013
Research

The influence of genomic context on mutation patterns in the human genome inferred from rare variants

  • First Published August 29, 2013
Method

Genotype calling and haplotyping in parent-offspring trios

  • First Published October 11, 2012
Research

Global DNA hypomethylation coupled to repressive chromatin domain formation and gene silencing in breast cancer

  • First Published December 7, 2011
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