ICR142 Benchmarker: evaluating, optimising and benchmarking variant calling performance using the ICR142 NGS validation series
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N. Rahman | S. Ellard | A. Renwick | Esty Holt | S. Mahamdallie | Elise Ruark | Márton Münz | Shawn E. Yost | M. Wakeling
[1] Donghe Li,et al. Comparison of INDEL Calling Tools with Simulation Data and Real Short-Read Data , 2019, IEEE/ACM Transactions on Computational Biology and Bioinformatics.
[2] S. Ellard,et al. Diagnosis of lethal or prenatal‐onset autosomal recessive disorders by parental exome sequencing , 2017, Prenatal diagnosis.
[3] Sarah Sandmann,et al. Evaluating Variant Calling Tools for Non-Matched Next-Generation Sequencing Data , 2017, Scientific Reports.
[4] Cory Y. McLean,et al. Creating a universal SNP and small indel variant caller with deep neural networks , 2016, bioRxiv.
[5] Nazneen Rahman,et al. OpEx - a validated, automated pipeline optimised for clinical exome sequence analysis , 2016, Scientific Reports.
[6] S. Seal,et al. The ICR142 NGS validation series: a resource for orthogonal assessment of NGS analysis , 2016, F1000Research.
[7] Ewa A. Bergmann,et al. Indel variant analysis of short-read sequencing data with Scalpel , 2015, Nature Protocols.
[8] Nazneen Rahman,et al. CSN and CAVA: variant annotation tools for rapid, robust next-generation sequencing analysis in the clinical setting , 2015, Genome Medicine.
[9] G. McVean,et al. Integrating mapping-, assembly- and haplotype-based approaches for calling variants in clinical sequencing applications , 2014, Nature Genetics.
[10] Heng Li,et al. Toward better understanding of artifacts in variant calling from high-coverage samples , 2014, Bioinform..
[11] Christopher A. Miller,et al. VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing. , 2012, Genome research.
[12] M. DePristo,et al. A framework for variation discovery and genotyping using next-generation DNA sequencing data , 2011, Nature Genetics.
[13] Alexis B. Carter,et al. Standards and Guidelines for Validating Next-Generation Sequencing Bioinformatics Pipelines: A Joint Recommendation of the Association for Molecular Pathology and the College of American Pathologists. , 2018, The Journal of molecular diagnostics : JMD.
[14] Sequence analysis Advance Access publication June 7, 2011 The variant call format and VCFtools , 2010 .