about
Integrative annotation of variants from 1092 humans: application to cancer genomicsTesting of candidate single nucleotide variants associated with paclitaxel neuropathy in the trial NCCTG N08C1 (Alliance)Mapping copy number variation by population-scale genome sequencingThe PsychENCODE projectCNVnator: an approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencingAn AP endonuclease 1-DNA polymerase beta complex: theoretical prediction of interacting surfacesAnalysis of variable retroduplications in human populations suggests coupling of retrotransposition to cell divisionPEMer: a computational framework with simulation-based error models for inferring genomic structural variants from massive paired-end sequencing dataA comprehensive analysis of non-sequential alignments between all protein structuresFOXG1-Dependent Dysregulation of GABA/Glutamate Neuron Differentiation in Autism Spectrum DisordersArchitecture of the human regulatory network derived from ENCODE dataTOPOFIT-DB, a database of protein structural alignments based on the TOPOFIT methodFriend, an integrated analytical front-end application for bioinformatics.Analysis of combinatorial regulation: scaling of partnerships between regulators with the number of governed targetsComprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans.Genome-wide mapping of copy number variation in humans: comparative analysis of high resolution array platforms.Structural alignment of proteins by a novel TOPOFIT method, as a superimposition of common volumes at a topomax point.An integrated map of structural variation in 2,504 human genomes.AGE: defining breakpoints of genomic structural variants at single-nucleotide resolution, through optimal alignments with gap excisionAnnual Research Review: The promise of stem cell research for neuropsychiatric disordersAlleleSeq: analysis of allele-specific expression and binding in a network framework.VarSim: a high-fidelity simulation and validation framework for high-throughput genome sequencing with cancer applications.MetaSV: an accurate and integrative structural-variant caller for next generation sequencing.Analysis of deletion breakpoints from 1,092 humans reveals details of mutation mechanisms.Regulatory element copy number differences shape primate expression profiles.Somatic copy number mosaicism in human skin revealed by induced pluripotent stem cells.A uniform survey of allele-specific binding and expression over 1000-Genomes-Project individuals.Colorectal Cancer with Residual Polyp of Origin: A Model of Malignant TransformationChild development and structural variation in the human genome.Landscape and variation of novel retroduplications in 26 human populations.Single-cell analysis of targeted transcriptome predicts drug sensitivity of single cells within human myeloma tumors.Integration of protein motions with molecular networks reveals different mechanisms for permanent and transient interactions.Human induced pluripotent stem cells for modelling neurodevelopmental disorders.Intersection of diverse neuronal genomes and neuropsychiatric disease: The Brain Somatic Mosaicism Network.Elevated variant density around SV breakpoints in germline lineage lends support to error-prone replication hypothesis.One thousand somatic SNVs per skin fibroblast cell set baseline of mosaic mutational load with patterns that suggest proliferative origin.UmuD and RecA directly modulate the mutagenic potential of the Y family DNA polymerase DinB.Structure SNP (StSNP): a web server for mapping and modeling nsSNPs on protein structures with linkage to metabolic pathways.Understanding genome structural variations.MSB: a mean-shift-based approach for the analysis of structural variation in the genome.
P50
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P50
description
hulumtues
@sq
onderzoeker
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researcher
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հետազոտող
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name
Alexej Abyzov
@ast
Alexej Abyzov
@en
Alexej Abyzov
@es
type
label
Alexej Abyzov
@ast
Alexej Abyzov
@en
Alexej Abyzov
@es
prefLabel
Alexej Abyzov
@ast
Alexej Abyzov
@en
Alexej Abyzov
@es
P106
P21
P2456
P31
P496
0000-0001-5405-6729