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Nature Communications|November 8, 2017
Mapping and phasing of structural variation in patient genomes using nanopore sequencingMircea Cretu Stancu, Markus J van Roosmalen, Ivo Renkens, et al.Frontiers in Immunology|September 12, 2025
Large-scale statistical mapping of T-cell receptor β sequences to human leukocyte antigensH Jabran Zahid, Ruth Taniguchi, Peter Ebert, et al.Cancers|March 29, 2023
Novel Generation of FAP Inhibitor-Based Homodimers for Improved Application in RadiotheranosticsMarcel Martin, Sanjana Ballal, Madhav Prasad Yadav, et al.Epigenetics & Chromatin|July 28, 2017
Regions of common inter-individual DNA methylation differences in human monocytes: genetic basis and potential functionChristopher Schröder, Elsa Leitão, Stefan Wallner, et al.Nature Biotechnology|December 8, 2020
Chromosome-scale, haplotype-resolved assembly of human genomesShilpa Garg, Arkarachai Fungtammasan, Andrew Carroll, et al.Nature Genetics|June 25, 2013
Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3Marcel Martin, Lars Maßhöfer, Petra Temming, et al.Cell Genomics|February 13, 2023
A multi-platform reference for somatic structural variation detectionJose Espejo Valle-Inclan, Nicolle J M Besselink, Ewart de Bruijn, et al.Nature Biotechnology|November 24, 2022
Functional analysis of structural variants in single cells using Strand-seqHyobin Jeong, Karen Grimes, Kerstin K Rauwolf, et al.Biorxiv : the Preprint Server for Biology|June 12, 2026
Population-scale Y chromosome assemblies reveal recurrent remodeling within constrained architecturesPille Hallast, Arang Rhie, Mark Loftus, et al.F1000Research|September 15, 2020
Sarek: A portable workflow for whole-genome sequencing analysis of germline and somatic variantsMaxime Garcia, Szilveszter Juhos, Malin Larsson, et al.Pageof 17