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Research

Rearrangements of viral and human genomes at human papillomavirus integration events and their allele-specific impacts on cancer genome regulation

  • First Published December 5, 2024
Method

Genome enrichment of rare and unknown species from complicated microbiomes by nanopore selective sequencing

  • First Published April 11, 2023
Method

Deep sequencing of short capped RNAs reveals novel families of noncoding RNAs

  • First Published August 12, 2022
Erratum

Erratum: Ultralow-input single-tube linked-read library method enables short-read second-generation sequencing systems to routinely generate highly accurate and economical long-range sequencing information

  • First Published May 3, 2021
Research

Comparative transcriptomics of primary cells in vertebrates

  • First Published July 27, 2020
Method

Ultralow-input single-tube linked-read library method enables short-read second-generation sequencing systems to routinely generate highly accurate and economical long-range sequencing information

  • First Published June 15, 2020
Research

High-resolution structural genomics reveals new therapeutic vulnerabilities in glioblastoma

  • First Published June 27, 2019
Research

The frequent evolutionary birth and death of functional promoters in mouse and human

  • First Published July 30, 2015
Method

TITAN: inference of copy number architectures in clonal cell populations from tumor whole-genome sequence data

  • First Published July 24, 2014
Method

Comparison of CAGE and RNA-seq transcriptome profiling using clonally amplified and single-molecule next-generation sequencing

  • First Published March 27, 2014
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