An integrative segmentation method for detecting germline copy number variations in SNP arrays.

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Bio-collections in autism research.Structural architecture of SNP effects on complex traits.A method for calling copy number polymorphism using haplotypes.VTET: a variable threshold exact test for identifying disease-associated copy number variations enriched in short genomic regions.

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P2860

An integrative segmentation method for detecting germline copy number variations in SNP arrays.

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http://www.wikidata.org/entity/Q43698193

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2012 nî lūn-bûn

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2012年学术文章

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An integrative segmentation me ...... mber variations in SNP arrays.

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An integrative segmentation me ...... mber variations in SNP arrays.

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An integrative segmentation me ...... mber variations in SNP arrays.

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An integrative segmentation me ...... mber variations in SNP arrays.

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An integrative segmentation me ...... mber variations in SNP arrays.

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An integrative segmentation me ...... mber variations in SNP arrays.

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P1476

An integrative segmentation me ...... mber variations in SNP arrays.

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P2093

Jianxin Shi

http://www.w3.org/2001/XMLSchema#string

Peng Li

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P2860

Rare chromosomal deletions and duplications increase risk of schizophrenia

A map of human genome variation from population-scale sequencing

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

Copy number variation at 1q21.1 associated with neuroblastoma

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

Circular binary segmentation for the analysis of array-based DNA copy number data

Comparative analysis of algorithms for identifying amplifications and deletions in array CGH data.

QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data.

Sparse representation and Bayesian detection of genome copy number alterations from microarray data.

Spatial smoothing and hot spot detection for CGH data using the fused lasso.

P304

373-383

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scholarly article

P356

10.1002/GEPI.21631

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2012-05-01T00:00:00Z

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224855728

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P698

22539397

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An integrative segmentation method for detecting germline copy number variations in SNP arrays.

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P2860

P2860

An integrative segmentation method for detecting germline copy number variations in SNP arrays.

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P1433

P1476

P2093

P2860

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P5875

P698

P356

P1433

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P2860

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P698