Cell Genomics is a new gold #OpenAccess and #OpenScience research journal that represents the forefront of #genetics and #genomics 馃К

Joined June 2020
Meet with us to discuss your research or to learn more about the publishing process! hubs.li/Q01msqBt0
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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: hubs.li/Q04B78lp0 #ImpactfulPaper
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NeoBridge: Biophysics-informed neoantigen prioritization and clonal architecture profiling in pancreatic cancer dlvr.鈥媔t/TVyG7G
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Detecting low-allele-fraction mosaic mutations: A multi-institution benchmarking with cell-line mixtures dlvr.鈥媔t/TVy8QS
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A pangenomic method for establishing a synthetic somatic variant resource in HapMap mixtures dlvr.鈥媔t/TVy58y
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Choice of phenotype scale is critical in biobank-based G 脳 E tests dlvr.鈥媔t/TVxnnw
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It鈥檚 been 5 years of Cell Genomics, and we鈥檙e celebrating! dlvr.鈥媔t/TVxhNl
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Deep learning uncovers hidden power of low-affinity motifs dlvr.鈥媔t/TVxWlW
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Establishing a genomic lab during COVID-19: A perspective from Institut Pasteur in C么te d鈥橧voire dlvr.鈥媔t/TVxRCZ
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Voices from contributors to Cell Genomics dlvr.鈥媔t/TVx2KB
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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. hubs.li/Q04BfKcr0
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Twelve voices from China: On publishing, community, and how the field of genomics is developing dlvr.鈥媔t/TVww7f
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Comments from the Cell Genomics board dlvr.鈥媔t/TVwlFS
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Mitotic and meiotic midbody remnants: Divergent architectures with distinct clinical applications dlvr.鈥媔t/TVwfQJ
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MOSHPIT: Accessible, reproducible metagenome data science on the QIIME 2 framework dlvr.鈥媔t/TVwFXP
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Intraspecific sequence variation and complete genomes refine the identification of rapidly evolved regions in humans dlvr.鈥媔t/TVw7SB
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This Cell Genomics paper shows how long-read sequencing improves detection and interpretation of structural and repeat variants in autism. Read the paper: hubs.li/Q04B73M80 #ImpactfulPaper
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Optimized parameters for CRISPR-Cas9 interference library design dlvr.鈥媔t/TVvycs
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RandomReadsMG: Rapid, realistic metagenome simulation at terabase scale for benchmarking and experimental design dlvr.鈥媔t/TVnMzG
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