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Centromeric instability and chromoanasynthesis observed in nine supernumerary marker chromosomes resolved with long-read genome sequencing

  • First Published March 25, 2026

Leveraging the T2T assembly to resolve rare and pathogenic inversions in reference genome gaps

  • First Published November 1, 2024

Resolving complex duplication variants in autism spectrum disorder using long-read genome sequencing

  • First Published October 29, 2024

A national long-read sequencing study on chromosomal rearrangements uncovers hidden complexities

  • First Published October 29, 2024

Gaps and complex structurally variant loci in phased genome assemblies

  • First Published May 10, 2023

Diversity, duplication, and genomic organization of homeobox genes in Lepidoptera

  • First Published December 8, 2022

Enhancers with tissue-specific activity are enriched in intronic regions

  • First Published July 21, 2021

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

  • First Published September 14, 2020

Chromatin activation as a unifying principle underlying pathogenic mechanisms in multiple myeloma

  • First Published August 20, 2020

A limited set of transcriptional programs define major cell types

  • First Published July 29, 2020
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