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Resource

Integrated single-cell multiome analysis reveals muscle fiber-type gene regulatory circuitry modulated by endurance exercise

  • First Published May 20, 2025
Method

Integration of transcriptomics and long-read genomics prioritizes structural variants in rare disease

  • First Published March 20, 2025
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
Corrigendum

Corrigendum: Functional annotation of human long noncoding RNAs via molecular phenotyping

  • First Published September 14, 2020
Resource

Functional annotation of human long noncoding RNAs via molecular phenotyping

  • First Published July 27, 2020
Research

Coexpression enrichment analysis at the single-cell level reveals convergent defects in neural progenitor cells and their cell-type transitions in neurodevelopmental disorders

  • First Published June 18, 2020
Method

cis-mediators for trans-eQTLs across many human tissues using genomic mediation analysis" > Identifying cis-mediators for trans-eQTLs across many human tissues using genomic mediation analysis

  • First Published October 11, 2017
Method

Co-expression networks reveal the tissue-specific regulation of transcription and splicing

  • First Published October 11, 2017
Research

Critical threshold levels of DNA methyltransferase 1 are required to maintain DNA methylation across the genome in human cancer cells

  • First Published February 23, 2017
Research

Impact of the X Chromosome and sex on regulatory variation

  • First Published April 21, 2016
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