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A deconvolution framework that uses single-cell sequencing plus a small benchmark data set for accurate analysis of cell type ratios in complex tissue samples

  • First Published November 25, 2024
Method

Accelerated somatic mutation calling for whole-genome and whole-exome sequencing data from heterogenous tumor samples

  • First Published April 8, 2024
Method

Analyzing rare mutations in metagenomes assembled using long and accurate reads

  • First Published November 23, 2022
Method

Fast and accurate mapping of long reads to complete genome assemblies with VerityMap

  • First Published November 15, 2022
Method

Automated annotation of human centromeres with HORmon

  • First Published May 11, 2022
Method

Variations in antibody repertoires correlate with vaccine responses

  • First Published March 31, 2022
Research

Deep sequencing of 1320 genes reveals the landscape of protein-truncating variants and their contribution to psoriasis in 19,973 Chinese individuals

  • First Published June 21, 2021
Method

A pedigree-based prediction model identifies carriers of deleterious de novo mutations in families with Li-Fraumeni syndrome

  • First Published August 18, 2020
Method

Plasmid detection and assembly in genomic and metagenomic data sets

  • First Published May 2, 2019
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