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Mismatch repair deficiency does not enhance ENU mutagenesis in the zebrafish germ line.Zebrafish with mutations in mismatch repair genes develop neurofibromas and other tumors.SambambaChromothripsis is a common mechanism driving genomic rearrangements in primary and metastatic colorectal cancerGenomic DNA pooling strategy for next-generation sequencing-based rare variant discovery in abdominal aortic aneurysm regions of interest-challenges and limitationsA Living Biobank of Breast Cancer Organoids Captures Disease HeterogeneityIncomplete segregation of MYH11 variants with thoracic aortic aneurysms and dissections and patent ductus arteriosusTargeted next-generation sequencingNext-generation sequencing-based genome diagnostics across clinical genetics centersHeterozygous KIDINS220/ARMS nonsense variants cause spastic paraplegia, intellectual disability, nystagmus, and obesitySimultaneous detection of clinically relevant mutations and amplifications for routine cancer pathologyTracing the history of goat pastoralism: new clues from mitochondrial and Y chromosome DNA in North AfricaImproved generation of rat gene knockouts by target-selected mutagenesis in mismatch repair-deficient animals.A systematic genome-wide analysis of zebrafish protein-coding gene functionIdentification of factors required for meristem function in Arabidopsis using a novel next generation sequencing fast forward genetics approachTissue-specific mutation accumulation in human adult stem cells during lifePrimary colorectal cancers and their subsequent hepatic metastases are genetically different: implications for selection of patients for targeted treatmentAccurate SNP and mutation detection by targeted custom microarray-based genomic enrichment of short-fragment sequencing librariesIdentification of genetic modifiers of behavioral phenotypes in serotonin transporter knockout ratsA hypomorphic mutation in Lpin1 induces progressively improving neuropathy and lipodystrophy in the ratGenomic and transcriptomic plasticity in treatment-naive ovarian cancerMutation discovery by targeted genomic enrichment of multiplexed barcoded samplesSingle nucleotide polymorphism (SNP) panels for rapid positional cloning in zebrafishEffector identification in the lettuce downy mildew Bremia lactucae by massively parallel transcriptome sequencingDiscovery of variants unmasked by hemizygous deletionsGenome-wide survey indicates involvement of loci on canine chromosomes 7 and 31 in patellar luxation in Flat-Coated RetrieversPhylogeny of Y chromosomes from bovine speciesMultiplexed array-based and in-solution genomic enrichment for flexible and cost-effective targeted next-generation sequencingOrganoid models of human and mouse ductal pancreatic cancerGenes unlinked to the leptin receptor influence urinary albumin excretion in obese Zucker ratsDual origins of dairy cattle farming--evidence from a comprehensive survey of European Y-chromosomal variationA genome-wide SNP panel for mapping and association studies in the rat.Effective Therapeutic Intervention and Comprehensive Genetic Analysis of mTOR Signaling in PEComaDominant missense mutations in ABCC9 cause Cantu syndromePrioritization and burden analysis of rare variants in 208 candidate genes suggest they do not play a major role in CAKUTSystematic generation of in vivo G protein-coupled receptor mutants in the ratGenetic etiology of renal agenesisGenome-wide pattern of TCF7L2/TCF4 chromatin occupancy in colorectal cancer cells.Next-generation sequencing-based genome diagnostics across clinical genetics centersLoss of syntaxin 3 causes variant microvillus inclusion disease