A crowdsourcing method for correcting sequencing errors for the third-generation sequencing data
暂无分享,去创建一个
Tian Zheng | Yixuan Wang | Yu Geng | Zhongmeng Zhao | Jiayin Wang | Xuanping Zhang | Siyu He | Zhaofang Du | Zhongmeng Zhao | Jiayin Wang | Xuanping Zhang | Yu Geng | Yixuan Wang | Tian Zheng | Zhaofang Du | Siyu He
[1] T Laver,et al. Assessing the performance of the Oxford Nanopore Technologies MinION , 2015, Biomolecular detection and quantification.
[2] Jan Schröder,et al. BIOINFORMATICS ORIGINAL PAPER , 2022 .
[3] Esko Ukkonen,et al. Accurate self-correction of errors in long reads using de Bruijn graphs , 2016, Bioinform..
[4] Jing Xu,et al. Accurately Estimating Tumor Purity of Samples with High Degree of Heterogeneity from Cancer Sequencing Data , 2017, ICIC.
[5] Jin Zhang,et al. An improved approach for accurate and efficient calling of structural variations with low-coverage sequence data , 2012, BMC Bioinformatics.
[6] Joshua F. McMichael,et al. Systematic Discovery of Complex Indels in Human Cancers , 2015, Nature medicine.
[7] Piet Demeester,et al. Jabba: hybrid error correction for long sequencing reads , 2015, Algorithms for Molecular Biology.
[8] Thomas Hackl,et al. proovread: large-scale high-accuracy PacBio correction through iterative short read consensus , 2014, Bioinform..
[9] Kiyoshi Asai,et al. PBSIM: PacBio reads simulator - toward accurate genome assembly , 2013, Bioinform..
[10] Aaron A. Klammer,et al. Nonhybrid, finished microbial genome assemblies from long-read SMRT sequencing data , 2013, Nature Methods.
[11] Joshua F. McMichael,et al. Age-related cancer mutations associated with clonal hematopoietic expansion , 2014, Nature Medicine.
[12] Jing Xu,et al. Identifying Heterogeneity Patterns of Allelic Imbalance on Germline Variants to Infer Clonal Architecture , 2017, ICIC.
[13] W. Wong,et al. Improving PacBio Long Read Accuracy by Short Read Alignment , 2012, PloS one.
[14] Hamid R. Rabiee,et al. A unified statistical framework for crowd labeling , 2015, Knowledge and Information Systems.
[15] Li Ding,et al. Patterns and functional implications of rare germline variants across 12 cancer types , 2015, Nature Communications.
[16] Glenn Tesler,et al. Mapping single molecule sequencing reads using basic local alignment with successive refinement (BLASR): application and theory , 2012, BMC Bioinformatics.
[17] J. Landolin,et al. Assembling Large Genomes with Single-Molecule Sequencing and Locality Sensitive Hashing , 2014 .
[18] Leena Salmela,et al. LoRDEC: accurate and efficient long read error correction , 2014, Bioinform..
[19] M. Schatz,et al. Hybrid error correction and de novo assembly of single-molecule sequencing reads , 2012, Nature Biotechnology.