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

  • First Published March 17, 2025

Integrating short-read and long-read single-cell RNA sequencing for comprehensive transcriptome profiling in mouse retina

  • First Published March 6, 2025

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

A deconvolution framework that uses single-cell sequencing plus a small benchmark data set for accurate analysis of cell type ratios in complex tissue samples

  • First Published November 25, 2024

CodonBERT large language model for mRNA vaccines

  • First Published July 1, 2024

Predicting unrecognized enhancer-mediated genome topology by an ensemble machine learning model

  • First Published November 12, 2020

Assembly and analysis of 100 full MHC haplotypes from the Danish population

  • First Published August 3, 2017

Systematic characterization of A-to-I RNA editing hotspots in microRNAs across human cancers

  • First Published April 14, 2017

SCRaMbLE generates designed combinatorial stochastic diversity in synthetic chromosomes

  • First Published November 13, 2015

Epigenetic modification and inheritance in sexual reversal of fish

  • First Published February 2, 2014
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