Detection of structural DNA variation from next generation sequencing data: a review of informatic approaches.
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Performance evaluation of indel calling tools using real short-read dataMulti-gene panel testing for hereditary cancer predisposition in unsolved high-risk breast and ovarian cancer patientsdigit-a tool for detection and identification of genomic interchromosomal translocationsA Path to Implement Precision Child Health Cardiovascular MedicineLinked read sequencing resolves complex genomic rearrangements in gastric cancer metastases.Detection of gene rearrangements in targeted clinical next-generation sequencing.High-throughput sequencing in mutation detection: A new generation of genotoxicity tests?Clinical implications of copy number variations in autoimmune disordersFunction of cancer associated genes revealed by modern univariate and multivariate association tests.ScanIndel: a hybrid framework for indel detection via gapped alignment, split reads and de novo assemblyIdentifying micro-inversions using high-throughput sequencing readsMolecular Characterization of Transgenic Events Using Next Generation Sequencing ApproachGenetic Evaluation of Schizophrenia Using the Illumina HumanExome ChipRepresenting genetic variation with synthetic DNA standards.Next-Generation Molecular Testing of Newborn Dried Blood Spots for Cystic FibrosisDevelopment and validation of a comprehensive genomic diagnostic tool for myeloid malignancies.Molecular diagnostics in soft tissue sarcomas and gastrointestinal stromal tumors.A new generation of cancer genome diagnostics for routine clinical use: overcoming the roadblocks to personalized cancer medicine.Whole-genome CNV analysis: advances in computational approachesMassive parallel sequencing of solid tumours - challenges and opportunities for pathologists.The role of genomics in common variable immunodeficiency disorders.Next-Generation Sequencing-Based Approaches for Mutation Mapping and Identification in Caenorhabditis elegans.Copy Number Variations in Amyotrophic Lateral Sclerosis: Piecing the Mosaic Tiles Together through a Systems Biology Approach.Goat domestication and breeding: a jigsaw of historical, biological and molecular data with missing pieces.Copy number variation and disease resistance in plants.Familial Cortical Myoclonic Tremor and Epilepsy, an Enigmatic Disorder: From Phenotypes to Pathophysiology and Genetics. A Systematic Review.Copy number changes of clinically actionable genes in melanoma, non-small cell lung cancer and colorectal cancer-A survey across 822 routine diagnostic cases.Clinical next-generation sequencing in patients with non-small cell lung cancer.Genome-Wide Analysis of Interchromosomal Interaction Probabilities Reveals Chained Translocations and Overrepresentation of Translocation Breakpoints in Genes in a Cutaneous T-Cell Lymphoma Cell Line.Atypical Presentation of Bilateral Retinoblastoma with Floaters and Sub-Internal Limiting Membrane Seeds in an 11-Year-Old Asian Indian MaleDetecting Copy Number Variation via Next Generation TechnologySEG - A Software Program for Finding Somatic Copy Number Alterations in Whole Genome Sequencing Data of Cancer
P2860
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P2860
Detection of structural DNA variation from next generation sequencing data: a review of informatic approaches.
description
2013 nî lūn-bûn
@nan
2013 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի նոյեմբերին 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
Detection of structural DNA va ...... view of informatic approaches.
@ast
Detection of structural DNA va ...... view of informatic approaches.
@en
type
label
Detection of structural DNA va ...... view of informatic approaches.
@ast
Detection of structural DNA va ...... view of informatic approaches.
@en
prefLabel
Detection of structural DNA va ...... view of informatic approaches.
@ast
Detection of structural DNA va ...... view of informatic approaches.
@en
P2860
P1433
P1476
Detection of structural DNA va ...... view of informatic approaches.
@en
P2093
Eric J Duncavage
Haley J Abel
P2860
P304
P356
10.1016/J.CANCERGEN.2013.11.002
P577
2013-11-20T00:00:00Z