Systematic biases in DNA copy number originate from isolation procedures
about
Genome-wide copy number profiling to detect gene amplifications in neural progenitor cellsNon-random DNA fragmentation in next-generation sequencing.Prevention, diagnosis and treatment of high-throughput sequencing data pathologies.Detecting and correcting systematic variation in large-scale RNA sequencing dataCopy number variation is a fundamental aspect of the placental genome.Patterns of sequencing coverage bias revealed by ultra-deep sequencing of vertebrate mitochondria.DNA isolation protocol effects on nuclear DNA analysis by microarrays, droplet digital PCR, and whole genome sequencing, and on mitochondrial DNA copy number estimation.SNP array profiling of mouse cell lines identifies their strains of origin and reveals cross-contamination and widespread aneuploidy.Genetic variation in human DNA replication timingLack of major genome instability in tumors of p53 null ratsIdentifying Human Genome-Wide CNV, LOH and UPD by Targeted Sequencing of Selected Regions.Gene amplification during differentiation of mammalian neural stem cells in vitro and in vivo.Deep landscape update of dispersed and tandem repeats in the genome model of the red jungle fowl, Gallus gallus, using a series of de novo investigating tools.CNARA: reliability assessment for genomic copy number profiles.Comparison of six commercial kits to extract bacterial chromosome and plasmid DNA for MiSeq sequencing.Identifying and mitigating bias in next-generation sequencing methods for chromatin biology.Whole exome association of rare deletions in multiplex oral cleft families.Measuring mutation accumulation in single human adult stem cells by whole-genome sequencing of organoid cultures.ACMG Standards and Guidelines for constitutional cytogenomic microarray analysis, including postnatal and prenatal applications: revision 2013.Optimal Fixation Conditions and DNA Extraction Methods for MLPA Analysis on FFPE Tissue-Derived DNA.Somatic mutations in neurons during aging and neurodegeneration.Plasmid-normalized quantification of relative mitochondrial DNA copy number
P2860
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P2860
Systematic biases in DNA copy number originate from isolation procedures
description
2013 nî lūn-bûn
@nan
2013 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Systematic biases in DNA copy number originate from isolation procedures
@ast
Systematic biases in DNA copy number originate from isolation procedures
@en
Systematic biases in DNA copy number originate from isolation procedures
@nl
type
label
Systematic biases in DNA copy number originate from isolation procedures
@ast
Systematic biases in DNA copy number originate from isolation procedures
@en
Systematic biases in DNA copy number originate from isolation procedures
@nl
prefLabel
Systematic biases in DNA copy number originate from isolation procedures
@ast
Systematic biases in DNA copy number originate from isolation procedures
@en
Systematic biases in DNA copy number originate from isolation procedures
@nl
P2093
P2860
P50
P3181
P356
P1433
P1476
Systematic biases in DNA copy number originate from isolation procedures
@en
P2093
James D Shull
Pim Toonen
Rajdeep Mehon
Timothy J Aitman
Veronika Boskova
Wade Junker
P2860
P2888
P3181
P356
10.1186/GB-2013-14-4-R33
P407
P577
2013-04-24T00:00:00Z
P5875
P6179
1021180900