about
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot projectChromosomal structural variations during progression of a prostate epithelial cell line to a malignant metastatic state inactivate the NF2, NIPSNAP1, UGT2B17, and LPIN2 genesBreakpoint profiling of 64 cancer genomes reveals numerous complex rearrangements spawned by homology-independent mechanisms.miR-99 family of MicroRNAs suppresses the expression of prostate-specific antigen and prostate cancer cell proliferation.Detection of DNA fusion junctions for BCR-ABL translocations by Anchored ChromPETA novel class of small RNAs: tRNA-derived RNA fragments (tRFs).Genomic study of replication initiation in human chromosomes reveals the influence of transcription regulation and chromatin structure on origin selection.Yeast genome analysis identifies chromosomal translocation, gene conversion events and several sites of Ty element insertion.Muscle-specific microRNA miR-206 promotes muscle differentiation.Targeted comparative RNA interference analysis reveals differential requirement of genes essential for cell proliferationPan-S replication patterns and chromosomal domains defined by genome-tiling arrays of ENCODE genomic areasSystems consequences of amplicon formation in human breast cancerAn integrated map of structural variation in 2,504 human genomes.Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences.Ploidy-Seq: inferring mutational chronology by sequencing polyploid tumor subpopulationsEfficient CRISPR/Cas9-Mediated Genome Editing in Mice by Zygote Electroporation of Nuclease.Abberantly placed impacted mandibular canine.Computational inference of a genomic pluripotency signature in human and mouse stem cells.Facile and rapid thermo-regulated biomineralization of gold by pullulan and study of its thermodynamic parameters.In-Ear Pulse Wave Measurements: A Pilot Study.Biosynthesis of gold and silver nanoparticles using a novel marine strain of Stenotrophomonas.FusorSV: an algorithm for optimally combining data from multiple structural variation detection methods.A Bayesian Framework for Generalized Linear Mixed Modeling Identifies New Candidate Loci for Late-Onset Alzheimer's Disease.Multi-platform discovery of haplotype-resolved structural variation in human genomes
P50
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P50
description
Forscher
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chercheur
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investigador
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onderzoeker
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researcher
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հետազոտող
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研究者
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name
Ankit Malhotra
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Ankit Malhotra
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Ankit Malhotra
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Ankit Malhotra
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type
label
Ankit Malhotra
@ast
Ankit Malhotra
@en
Ankit Malhotra
@es
Ankit Malhotra
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prefLabel
Ankit Malhotra
@ast
Ankit Malhotra
@en
Ankit Malhotra
@es
Ankit Malhotra
@nl
P106
P31
P496
0000-0002-1905-0732