about
Genome sequence of the Brown Norway rat yields insights into mammalian evolutionMolecular cloning and mapping of human semaphorin F from the Cri-du-chat candidate intervalIdentification of genes expressed by immune cells of the colon that are regulated by colorectal cancer-associated variantsSpectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation.Pancreatic cancer genomes reveal aberrations in axon guidance pathway genesCharacterizing the cancer genome in lung adenocarcinoma.Lineage-specific expansions of retroviral insertions within the genomes of African great apes but not humans and orangutansThe male-specific region of the human Y chromosome is a mosaic of discrete sequence classesThe DNA sequence and analysis of human chromosome 14A high-resolution map of human chromosome 12Human aldehyde dehydrogenase: chromosomal assignment of the gene for the isozyme that metabolizes gamma-aminobutyraldehydeLocalization of the D5 dopamine receptor gene to human chromosome 4p15.1-p15.3, centromeric to the Huntington's disease locusFine mapping of chromosome 5p15.33 based on a targeted deep sequencing and high density genotyping identifies novel lung cancer susceptibility lociGenomic Support for a Moa-Tinamou Clade and Adaptive Morphological Convergence in Flightless RatitesHotspot activating PRKD1 somatic mutations in polymorphous low-grade adenocarcinomas of the salivary glands.A renewed model of pancreatic cancer evolution based on genomic rearrangement patternsOptimization of miRNA-seq data preprocessing.Integrated and sequence-ordered BAC- and YAC-based physical maps for the rat genome.Fosmid-based physical mapping of the Histoplasma capsulatum genomeIdentification of novel high-frequency DNA methylation changes in breast cancerThe completion of the Mammalian Gene Collection (MGC).The GAAS metagenomic tool and its estimations of viral and microbial average genome size in four major biomes.Punctuated duplication seeding events during the evolution of human chromosome 2p11.Next-generation sequencing identifies rare variants associated with Noonan syndromeFeasibility of real time next generation sequencing of cancer genes linked to drug response: results from a clinical trial.A physical map of the mouse genome.Unraveling the genetics of cancer: genome sequencing and beyond.Somatic cell mapping of the human cyclophilin B gene (PPIB) to chromosome 15.Identification of pre-leukaemic haematopoietic stem cells in acute leukaemia.Coming of age: ten years of next-generation sequencing technologies.Comprehensive DNA methylation profiling in a human cancer genome identifies novel epigenetic targets.Demographic histories and patterns of linkage disequilibrium in Chinese and Indian rhesus macaques.Software for automated analysis of DNA fingerprinting gels.The LN54 radiation hybrid map of zebrafish expressed sequences.Use of Sequenom sample ID Plus® SNP genotyping in identification of FFPE tumor samples.ShatterProof: operational detection and quantification of chromothripsis.A two-dimensional pooling strategy for rare variant detection on next-generation sequencing platforms.A cancer cell-line titration series for evaluating somatic classification.Massively parallel bisulphite pyrosequencing reveals the molecular complexity of breast cancer-associated cytosine-methylation patterns obtained from tissue and serum DNA.A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing.
P50
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P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
John McPherson
@ast
John McPherson
@en
John McPherson
@es
John McPherson
@nl
John McPherson
@sl
type
label
John McPherson
@ast
John McPherson
@en
John McPherson
@es
John McPherson
@nl
John McPherson
@sl
altLabel
McPherson JD
@en
prefLabel
John McPherson
@ast
John McPherson
@en
John McPherson
@es
John McPherson
@nl
John McPherson
@sl
P1053
D-2633-2017
P106
P1153
7102659159
P21
P31
P3829
P496
0000-0001-8049-9347