Pages that link to "Q21284304"
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The following pages link to Computational tools for copy number variation (CNV) detection using next-generation sequencing data: features and perspectives (Q21284304):
Displaying 50 items.
- Retinal dystrophies, genomic applications in diagnosis and prospects for therapy (Q26770321) (← links)
- Not All Next Generation Sequencing Diagnostics are Created Equal: Understanding the Nuances of Solid Tumor Assay Design for Somatic Mutation Detection (Q26801745) (← links)
- Detection of Genomic Structural Variants from Next-Generation Sequencing Data (Q28082859) (← links)
- Somatic mosaicism for copy-neutral loss of heterozygosity and DNA copy number variations in the human genome (Q28388948) (← links)
- DNA Sequence Evolution and Rare Homoeologous Conversion in Tetraploid Cotton (Q28834391) (← links)
- Combined examination of sequence and copy number variations in human deafness genes improves diagnosis for cases of genetic deafness (Q30427880) (← links)
- ADaCGH2: parallelized analysis of (big) CNA data. (Q30758172) (← links)
- MOABS: model based analysis of bisulfite sequencing data (Q30763690) (← links)
- Combinatorial approach to estimate copy number genotype using whole-exome sequencing data (Q30881665) (← links)
- Detecting copy-number variations in whole-exome sequencing data using the eXome Hidden Markov Model: an 'exome-first' approach (Q30885441) (← links)
- CNOGpro: detection and quantification of CNVs in prokaryotic whole-genome sequencing data (Q30887163) (← links)
- An integrated approach for analyzing clinical genomic variant data from next-generation sequencing. (Q30887413) (← links)
- G-CNV: A GPU-Based Tool for Preparing Data to Detect CNVs with Read-Depth Methods. (Q30915634) (← links)
- CNV-CH: A Convex Hull Based Segmentation Approach to Detect Copy Number Variations (CNV) Using Next-Generation Sequencing Data (Q30988364) (← links)
- SAAS-CNV: A Joint Segmentation Approach on Aggregated and Allele Specific Signals for the Identification of Somatic Copy Number Alterations with Next-Generation Sequencing Data (Q31026307) (← links)
- cnvScan: a CNV screening and annotation tool to improve the clinical utility of computational CNV prediction from exome sequencing data (Q31036780) (← links)
- CoNVaDING: Single Exon Variation Detection in Targeted NGS Data (Q31044157) (← links)
- Rapid and powerful detection of subtle allelic imbalance from exome sequencing data with hapLOHseq (Q31107369) (← links)
- Methylotrophic methanogenesis discovered in the archaeal phylum Verstraetearchaeota (Q31134331) (← links)
- -Omic and Electronic Health Record Big Data Analytics for Precision Medicine (Q31136593) (← links)
- A statistical approach to detection of copy number variations in PCR-enriched targeted sequencing data (Q31138439) (← links)
- SeqCNV: a novel method for identification of copy number variations in targeted next-generation sequencing data (Q31169803) (← links)
- Multi-gene panel testing for hereditary cancer predisposition in unsolved high-risk breast and ovarian cancer patients (Q33618262) (← links)
- Circulating Tumor DNA Mutation Profiling by Targeted Next Generation Sequencing Provides Guidance for Personalized Treatments in Multiple Cancer Types (Q33673752) (← links)
- Gene-based comparative analysis of tools for estimating copy number alterations using whole-exome sequencing data (Q33689015) (← links)
- Multiplexed direct genomic selection (MDiGS): a pooled BAC capture approach for highly accurate CNV and SNP/INDEL detection (Q33698461) (← links)
- Novel variant in the FGD1 gene causing Aarskog-Scott syndrome (Q33744917) (← links)
- An evaluation of copy number variation detection tools for cancer using whole exome sequencing data (Q33750378) (← links)
- A novel network regularized matrix decomposition method to detect mutated cancer genes in tumour samples with inter-patient heterogeneity. (Q33767347) (← links)
- Copy number variants are a common cause of non-syndromic hearing loss (Q33796395) (← links)
- Automation of molecular-based analyses: a primer on massively parallel sequencing (Q34376481) (← links)
- Copy number variations in a population-based study of Charcot-Marie-Tooth disease (Q35013000) (← links)
- Rapid detection of structural variation in a human genome using nanochannel-based genome mapping technology (Q35066595) (← links)
- Copy number variations among silkworms (Q35135590) (← links)
- BamBam: genome sequence analysis tools for biologists (Q35447237) (← links)
- Quantitative analysis of differences in copy numbers using read depth obtained from PCR-enriched samples and controls (Q35550039) (← links)
- Genome Wide Distributions and Functional Characterization of Copy Number Variations between Chinese and Western Pigs (Q35685874) (← links)
- Copy number variants, aneuploidies, and human disease (Q35694174) (← links)
- Family-Based Benchmarking of Copy Number Variation Detection Software (Q35702888) (← links)
- VEGAWES: variational segmentation on whole exome sequencing for copy number detection (Q35790928) (← links)
- cnvCurator: an interactive visualization and editing tool for somatic copy number variations (Q35809613) (← links)
- The distribution and impact of common copy-number variation in the genome of the domesticated apple, Malus x domestica Borkh. (Q35817838) (← links)
- Genomic population structure and prevalence of copy number variations in South African Nguni cattle (Q35831304) (← links)
- CNVkit: Genome-Wide Copy Number Detection and Visualization from Targeted DNA Sequencing. (Q35995950) (← links)
- Genome-wide patterns of copy number variation in the Chinese yak genome (Q36024352) (← links)
- Copy number alterations detected by whole-exome and whole-genome sequencing of esophageal adenocarcinoma (Q36062064) (← links)
- Concordance of copy number loss and down-regulation of tumor suppressor genes: a pan-cancer study (Q36111351) (← links)
- CNARA: reliability assessment for genomic copy number profiles (Q36161725) (← links)
- Detection and validation of structural variations in bovine whole-genome sequence data (Q36260039) (← links)
- Segmentum: a tool for copy number analysis of cancer genomes (Q36346318) (← links)