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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
Method

Assessing and mitigating privacy risks of sparse, noisy genotypes by local alignment to haplotype databases

  • First Published December 14, 2023
Research

Comprehensive analysis of structural variants in breast cancer genomes using single-molecule sequencing

  • First Published September 4, 2020
Research

Human papillomavirus and the landscape of secondary genetic alterations in oral cancers

  • First Published December 18, 2018
Research

Complex rearrangements and oncogene amplifications revealed by long-read DNA and RNA sequencing of a breast cancer cell line

  • First Published June 28, 2018
Resource

A comparative transcriptional landscape of maize and sorghum obtained by single-molecule sequencing

  • First Published April 30, 2018
Research

Dynamic RNA–protein interactions underlie the zebrafish maternal-to-zygotic transition

  • First Published April 5, 2017
Research

Pangolin genomes and the evolution of mammalian scales and immunity

  • First Published August 10, 2016
Method

Oxford Nanopore sequencing, hybrid error correction, and de novo assembly of a eukaryotic genome

  • First Published October 7, 2015
Research

Genome-wide analysis of HPV integration in human cancers reveals recurrent, focal genomic instability

  • First Published November 7, 2013
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