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Resource

An integrative TAD catalog in lymphoblastoid cell lines discloses the functional impact of deletions and insertions in human genomes

  • First Published December 5, 2024
Resource

High-coverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalog of human genetic variation

  • First Published October 2, 2024
Method

Whole-genome bisulfite sequencing with improved accuracy and cost

  • First Published August 9, 2018
Method

taxMaps: comprehensive and highly accurate taxonomic classification of short-read data in reasonable time

  • First Published March 27, 2018
Resource

Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly

  • First Published April 10, 2017
Method

Using reference-free compressed data structures to analyze sequencing reads from thousands of human genomes

  • First Published December 16, 2016
Resource

Assemblathon 1: A competitive assessment of de novo short read assembly methods

  • First Published September 16, 2011
Method

Revealing the genetic structure of a trait by sequencing a population under selection

  • First Published March 21, 2011
Resource

ABySS: A parallel assembler for short read sequence data

  • First Published February 27, 2009
LETTER

Why do human diversity levels vary at a megabase scale?

  • First Published September 1, 2005
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