Single-cell phylogenies reveal deviations from clock-like, neutral evolution in cancer and healthy tissues | bioRxiv
PDF) Analysis of the Batch Effect Due to Sequencing Center in Population Statistics Quantifying Rare Events in the 1000 Genomes Project
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk | Nature Genetics
IJMS | Free Full-Text | Genomic, Clinical, and Behavioral Characterization of 15q11.2 BP1-BP2 Deletion (Burnside-Butler) Syndrome in Five Families
Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes | Nature Medicine
IJMS | Free Full-Text | Whole-Genome Sequencing of 502 Individuals from Latvia: The First Step towards a Population-Specific Reference of Genetic Variation
IJMS | Free Full-Text | Whole-Genome Sequencing of 502 Individuals from Latvia: The First Step towards a Population-Specific Reference of Genetic Variation
Requirements for comprehensive pharmacogenetic genotyping platforms | Pharmacogenomics
A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes | Science
An Omic and Multidimensional Spatial Atlas from Serial Biopsies of an Evolving Metastatic Breast Cancer | bioRxiv
Whole-genome landscape of mucosal melanoma reveals diverse drivers and therapeutic targets | Nature Communications
Genes | Free Full-Text | Genetic Characterization of Blood Group Antigens for Polynesian Heritage Norfolk Island Residents
GCAT|Panel, a comprehensive structural variant haplotype map of the Iberian population from high-coverage whole-genome sequencing | bioRxiv
Proteomic Analysis of Whole Blood Using Volumetric Absorptive Microsampling for Precision Medicine Biomarker Studies | Journal of Proteome Research
Sequence data and association statistics from 12,940 type 2 diabetes cases and controls | Scientific Data
GCAT|Panel, a comprehensive structural variant haplotype map of the Iberian population from high-coverage whole-genome sequencing | bioRxiv
Genes | Free Full-Text | Whole Exome Sequencing Reveals Novel Candidate Genes in Familial Forms of Glaucomatous Neurodegeneration
Frontiers | Distinct microRNA and protein profiles of extracellular vesicles secreted from myotubes from morbidly obese donors with type 2 diabetes in response to electrical pulse stimulation
SIEVE: joint inference of single-nucleotide variants and cell phylogeny from single-cell DNA sequencing data | bioRxiv
An Omic and Multidimensional Spatial Atlas from Serial Biopsies of an Evolving Metastatic Breast Cancer | bioRxiv
GCAT|Panel, a comprehensive structural variant haplotype map of the Iberian population from high-coverage whole-genome sequencing | bioRxiv
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Whole-genome landscape of mucosal melanoma reveals diverse drivers and therapeutic targets | Nature Communications
Genes | Free Full-Text | Rare Variant Analysis and Molecular Dynamics Simulation in Alzheimer’s Disease Identifies Exonic Variants in FLG
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Genes | Free Full-Text | Analysis of the Batch Effect Due to Sequencing Center in Population Statistics Quantifying Rare Events in the 1000 Genomes Project
