Your search for returned 31 results

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Research

Characterizing cytosine methylation of polymorphic transposable element insertions using the human pangenome resources

  • First Published May 14, 2026
Method

Verkko2 integrates proximity-ligation data with long-read De Bruijn graphs for efficient telomere-to-telomere genome assembly, phasing, and scaffolding

  • First Published May 19, 2025
Method

Highly accurate assembly polishing with DeepPolisher

  • First Published May 19, 2025
Method

HiCanu: accurate assembly of segmental duplications, satellites, and allelic variants from high-fidelity long reads

  • First Published August 14, 2020
Method

Ancestry-agnostic estimation of DNA sample contamination from sequence reads

  • First Published January 24, 2020
Method

Canu: scalable and accurate long-read assembly via adaptive k-mer weighting and repeat separation

  • First Published March 15, 2017
Method

Read clouds uncover variation in complex regions of the human genome

  • First Published August 18, 2015
Method

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

  • First Published April 16, 2015
Method

Discovery of recurrent structural variants in nasopharyngeal carcinoma

  • First Published November 8, 2013
Research

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

  • First Published August 29, 2013
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