Your search for returned 37 results

Order by:
Show per page
Review

Leveraging the power of long reads for targeted sequencing

  • First Published November 20, 2024
Method

Gapless assembly of complete human and plant chromosomes using only nanopore sequencing

  • First Published November 6, 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
Research

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

  • First Published September 4, 2020
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
Method

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

  • First Published October 7, 2015
Resource

Sequence features and chromatin structure around the genomic regions bound by 119 human transcription factors

  • First Published September 5, 2012
Research

Understanding transcriptional regulation by integrative analysis of transcription factor binding data

  • First Published September 5, 2012
Research

Cell-type specific and combinatorial usage of diverse transcription factors revealed by genome-wide binding studies in multiple human cells

  • First Published November 16, 2011
Show per page