Your search for returned 45 results

Order by:
Show per page
Resource

Lignature provides a curated resource of ligand induced transcriptomic signatures for signaling inference

  • First Published April 8, 2026
Method

Highly accurate assembly polishing with DeepPolisher

  • First Published May 19, 2025
Method

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

  • First Published March 20, 2025
Perspective

Unraveling the hidden complexity of cancer through long-read sequencing

  • First Published March 20, 2025
Research

Closing the gaps, and improving somatic structural variant analysis and benchmarking using CHM13-T2T

  • First Published March 17, 2025
Review

k-mer approaches for biodiversity genomics" > k-mer approaches for biodiversity genomics

  • First Published January 31, 2025
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

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

Differences in activity and stability drive transposable element variation in tropical and temperate maize

  • First Published September 9, 2024
Show per page