A single-sample method for normalizing and combining full-resolution copy numbers from multiple platforms, labs and analysis methods.
about
arrayMap: a reference resource for genomic copy number imbalances in human malignanciesThe pitfalls of platform comparison: DNA copy number array technologies assessed.TumorBoost: normalization of allele-specific tumor copy numbers from a single pair of tumor-normal genotyping microarraysJoint estimation of DNA copy number from multiple platformsA novel SNP analysis method to detect copy number alterations with an unbiased reference signal directly from tumor samples.A new highly penetrant form of obesity due to deletions on chromosome 16p11.2.Transcriptional profile of tuberculosis antigen-specific T cells reveals novel multifunctional featuresCharacterization of colon cancer cells: a functional approach characterizing CD133 as a potential stem cell markerMirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.Visualization of genomic changes by segmented smoothing using an L0 penaltyIdentification and validation of copy number variants using SNP genotyping arrays from a large clinical cohortIntegrative genome-wide expression profiling identifies three distinct molecular subgroups of renal cell carcinoma with different patient outcomeSimple binary segmentation frameworks for identifying variation in DNA copy number.Identification of rare DNA variants in mitochondrial disorders with improved array-based sequencing.Suppression of lung adenocarcinoma progression by Nkx2-1Tolerance of whole-genome doubling propagates chromosomal instability and accelerates cancer genome evolution.Parent-specific copy number in paired tumor-normal studies using circular binary segmentationAlterations of LKB1 and KRAS and risk of brain metastasis: comprehensive characterization by mutation analysis, copy number, and gene expression in non-small-cell lung carcinoma.Improved multiplex ligation-dependent probe amplification analysis identifies a deleterious PMS2 allele generated by recombination with crossover between PMS2 and PMS2CL.An integrated systems biology approach identifies positive cofactor 4 as a factor that increases reprogramming efficiency.A single-array preprocessing method for estimating full-resolution raw copy numbers from all Affymetrix genotyping arrays including GenomeWideSNP 5 & 6.Preprocessing and downstream analysis of microarray DNA copy number profiles.Tumor Evolution of Glioma-Intrinsic Gene Expression Subtypes Associates with Immunological Changes in the Microenvironment.
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A single-sample method for normalizing and combining full-resolution copy numbers from multiple platforms, labs and analysis methods.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 04 February 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
A single-sample method for nor ...... ms, labs and analysis methods.
@en
A single-sample method for nor ...... ms, labs and analysis methods.
@nl
type
label
A single-sample method for nor ...... ms, labs and analysis methods.
@en
A single-sample method for nor ...... ms, labs and analysis methods.
@nl
prefLabel
A single-sample method for nor ...... ms, labs and analysis methods.
@en
A single-sample method for nor ...... ms, labs and analysis methods.
@nl
P2860
P356
P1433
P1476
A single-sample method for nor ...... ms, labs and analysis methods.
@en
P2093
Amrita Ray
Paul Spellman
P2860
P304
P356
10.1093/BIOINFORMATICS/BTP074
P407
P577
2009-02-04T00:00:00Z