Cell Genomics

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TFXcan reveals transcription factor programs driving GWAS loci dlvr.​it/TW4jdL

Where a cell sits in a tissue matters. This Cell Genomics paper uses spatial transcriptomics to reveal altered cell communities and drivers of aberrant epithelia and pro-fibrotic fibroblasts in interstitial lung diseases. #ImpactfulPaper

Genetic differences can act differently from one cell type to the next. This Cell Genomics paper uses single-cell eQTL mapping to reveal cell-type-specific genetic regulation in lung cancer. One of our most-read papers: #ImpactfulPaper

NeoBridge: Biophysics-informed neoantigen prioritization and clonal architecture profiling in pancreatic cancer dlvr.​it/TVyG7G

Detecting low-allele-fraction mosaic mutations: A multi-institution benchmarking with cell-line mixtures dlvr.​it/TVy8QS

A pangenomic method for establishing a synthetic somatic variant resource in HapMap mixtures dlvr.​it/TVy58y

Choice of phenotype scale is critical in biobank-based G × E tests dlvr.​it/TVxnnw

It’s been 5 years of Cell Genomics, and we’re celebrating! dlvr.​it/TVxhNl

Deep learning uncovers hidden power of low-affinity motifs dlvr.​it/TVxWlW

Establishing a genomic lab during COVID-19: A perspective from Institut Pasteur in Côte d’Ivoire dlvr.​it/TVxRCZ

Voices from contributors to Cell Genomics dlvr.​it/TVx2KB

Celebrating 5 years of Cell Genomics! Explore our anniversary issue where contributors from around the world reflect on their research, their experiences with the journal, and the advances they hope to see over the next 5 years.

Twelve voices from China: On publishing, community, and how the field of genomics is developing dlvr.​it/TVww7f

Comments from the Cell Genomics board dlvr.​it/TVwlFS

Mitotic and meiotic midbody remnants: Divergent architectures with distinct clinical applications dlvr.​it/TVwfQJ

MOSHPIT: Accessible, reproducible metagenome data science on the QIIME 2 framework dlvr.​it/TVwFXP

Intraspecific sequence variation and complete genomes refine the identification of rapidly evolved regions in humans dlvr.​it/TVw7SB

This Cell Genomics paper shows how long-read sequencing improves detection and interpretation of structural and repeat variants in autism. Read the paper: #ImpactfulPaper

Optimized parameters for CRISPR-Cas9 interference library design dlvr.​it/TVvycs

RandomReadsMG: Rapid, realistic metagenome simulation at terabase scale for benchmarking and experimental design dlvr.​it/TVnMzG