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MILOSAVLJEVIC, ALEKSANDAR

One or more keywords matched the following properties of MILOSAVLJEVIC, ALEKSANDAR

Property	Value
keywords	Epigenome Epigenetics Genome Genomics Bioinformatics cancer genomics clinical genomics computational biology

One or more keywords matched the following items that are connected to MILOSAVLJEVIC, ALEKSANDAR

Item Type	Name
Academic Article	Discovering distinct genes represented in 29,570 clones from infant brain cDNA libraries by applying sequencing by hybridization methodology.
Academic Article	Prototypic sequences for human repetitive DNA.
Academic Article	Genome-scale DNA sequence recognition by hybridization to short oligomers.
Academic Article	Pash: efficient genome-scale sequence anchoring by Positional Hashing.
Academic Article	Pooled genomic indexing of rhesus macaque.
Academic Article	Genome sequence of the Brown Norway rat yields insights into mammalian evolution.
Academic Article	A sequence-level map of chromosomal breakpoints in the MCF-7 breast cancer cell line yields insights into the evolution of a cancer genome.
Academic Article	Clone-array pooled shotgun mapping and sequencing: design and analysis of experiments.
Academic Article	ReadDepth: a parallel R package for detecting copy number alterations from short sequencing reads.
Academic Article	Discovering functional modules by identifying recurrent and mutually exclusive mutational patterns in tumors.
Academic Article	A genome-wide search for promoters that respond to increased MYCN reveals both new oncogenic and tumor suppressor microRNAs associated with aggressive neuroblastoma.
Academic Article	Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE.
Academic Article	Atlas2 Cloud: a framework for personal genome analysis in the cloud.
Academic Article	Polymorphic microsatellite loci for the common marmoset (Callithrix jacchus) designed using a cost- and time-efficient method.
Academic Article	Abundance and length of simple repeats in vertebrate genomes are determined by their structural properties.
Academic Article	Long-range massively parallel mate pair sequencing detects distinct mutations and similar patterns of structural mutability in two breast cancer cell lines.
Academic Article	The NIH Roadmap Epigenomics Mapping Consortium.
Academic Article	An integrative variant analysis suite for whole exome next-generation sequencing data.
Academic Article	Pash 3.0: A versatile software package for read mapping and integrative analysis of genomic and epigenomic variation using massively parallel DNA sequencing.
Academic Article	Genomic hypomethylation in the human germline associates with selective structural mutability in the human genome.
Academic Article	Functional annotation of the human brain methylome identifies tissue-specific epigenetic variation across brain and blood.
Academic Article	Emerging patterns of epigenomic variation.
Academic Article	Spark: a navigational paradigm for genomic data exploration.
Academic Article	Confounding by repetitive elements and CpG islands does not explain the association between hypomethylation and genomic instability.
Academic Article	The DNA sequence, annotation and analysis of human chromosome 3.
Academic Article	The genome of the sea urchin Strongylocentrotus purpuratus.
Academic Article	A high-resolution map of synteny disruptions in gibbon and human genomes.
Academic Article	Evolutionary and biomedical insights from the rhesus macaque genome.
Academic Article	Human-specific changes of genome structure detected by genomic triangulation.
Academic Article	Pash 2.0: scaleable sequence anchoring for next-generation sequencing technologies.
Academic Article	Evolutionary breakpoints in the gibbon suggest association between cytosine methylation and karyotype evolution.
Academic Article	Centromere remodeling in Hoolock leuconedys (Hylobatidae) by a new transposable element unique to the gibbons.
Academic Article	ChIP-seq guidelines and practices of the ENCODE and modENCODE consortia.
Concept	Human Genome Project
Concept	Genome, Human
Concept	Genome, Bacterial
Concept	Genome-Wide Association Study
Concept	Genome
Academic Article	NAHR-mediated copy-number variants in a clinical population: mechanistic insights into both genomic disorders and Mendelizing traits.
Academic Article	Recommendations for the design and analysis of epigenome-wide association studies.
Academic Article	Comparison and quantitative verification of mapping algorithms for whole-genome bisulfite sequencing.
Academic Article	Analysis of interactions between the epigenome and structural mutability of the genome using Genboree Workbench tools.
Academic Article	Intermediate DNA methylation is a conserved signature of genome regulation.
Academic Article	Integrative analysis of 111 reference human epigenomes.
Academic Article	Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium.
Academic Article	ClinGen Pathogenicity Calculator: a configurable system for assessing pathogenicity of genetic variants.
Academic Article	Allele-specific epigenome maps reveal sequence-dependent stochastic switching at regulatory loci.
Academic Article	ClinGen advancing genomic data-sharing standards as a GA4GH driver project.
Grant	Epigenomics 2015: A Roadmap to the Living Genome
Grant	Clone-Array Pooled Shotgun Indexing
Grant	The pluripotency regulator Prdm14 initiates cancer by epigenetic mechanisms
Grant	Multiplexed Methods for the Study of Chromosomal Aberrations in Cancer
Grant	Genboree System for Translational Studies of Genome Variation
Grant	Comprehensive High-throughput Mapping of Cancer Genomes
Grant	Clone Pooling Methods for Physical Mapping
Grant	Epigenomics Data Analysis and Coordination Center at Baylor College of Medicine
Grant	DATA MANAGEMENT AND RESOURCE REPOSITORY FOR THE exRNA ATLAS PHASE II
Grant	Baylor College of Medicine/Stanford University Clinical Genome Resource (CLINGEN)
Academic Article	The EN-TEx resource of multi-tissue personal epigenomes?& variant-impact models.

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Genome