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De novo detection of somatic variants in high-quality long-read single-cell RNA sequencing data

  • First Published March 19, 2025

Accurate fusion transcript identification from long- and short-read isoform sequencing at bulk or single-cell resolution

  • First Published March 14, 2025

Accurate sequencing of DNA motifs able to form alternative (non-B) structures

  • First Published July 11, 2023

Selection and thermostability suggest G-quadruplexes are novel functional elements of the human genome

  • First Published June 29, 2021

Long-read sequencing technology indicates genome-wide effects of non-B DNA on polymerization speed and error rate

  • First Published November 6, 2018

Single-cell sequencing data reveal widespread recurrence and loss of mutational hits in the life histories of tumors

  • First Published October 13, 2017

Corrigendum: A genome-wide analysis of common fragile sites: What features determine chromosomal instability in the human genome?

  • First Published October 3, 2016

A genome-wide analysis of common fragile sites: What features determine chromosomal instability in the human genome?

  • First Published March 28, 2012

A matter of life or death: How microsatellites emerge in and vanish from the human genome

  • First Published October 12, 2011

Dynamics of the epigenetic landscape during erythroid differentiation after GATA1 restoration

  • First Published July 27, 2011
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