Tom Skelly

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Distinguishing highly similar gene isoforms with a clustering-based bioinformatics analysis of PacBio single-molecule long reads

Qiang Sun, Bin Zhou, Xin Zheng, 2016, BioData Mining.

Consortium, G.P A map of human genome variation from population-scale sequencing. Nature 467, 1061-1073

Ken Chen, Joshua M. Korn, Afidalina Tumian, 2010 .

Towards Better Precision Medicine: PacBio Single-Molecule Long Reads Resolve the Interpretation of HIV Drug Resistant Mutation Profiles at Explicit Quasispecies (Haplotype) Level

Liang Ma, Castle Raley, Brad T. Sherman, 2015, Journal of data mining in genomics & proteomics.

SASI-Seq: sample assurance Spike-Ins, and highly differentiating 384 barcoding for Illumina sequencing

Steven Leonard, Michael A Quail, H. Swerdlow, 2014, BMC Genomics.

Optimal enzymes for amplifying sequencing libraries

Michael A Quail, Thomas D Otto, Simon R Harris, 2011, Nature Methods.

Exploratory analysis and error modeling of a sequencing technology

Irina I. Abnizova, Heng Li, Tom Skelly, 2016, bioRxiv.

Swift: primary data analysis for the Illumina Solexa sequencing platform

Irina I. Abnizova, Alexander Wait Zaranek, Tom Skelly, 2009, Bioinform..

Distinguishing highly similar gene isoforms with a clustering-based bioinformatics analysis of PacBio single-molecule long reads

Robert M. Stephens, B. Sherman, W. Lau, 2016, BioData Mining.

Statistical Comparison of Methods to Estimate the Error Probability in Short-Read Illumina Sequencing

Irina I. Abnizova, Tom Skelly, Fedor Naumenko, 2010, J. Bioinform. Comput. Biol..

Analysis of Context-Dependent Errors for Illumina sequencing

Andy Brown, I. René J. A. te Boekhorst, Irina I. Abnizova, 2012, J. Bioinform. Comput. Biol..

Optimal enzymes for amplifying sequencing libraries

H. Swerdlow, M. Quail, S. Harris, 2011, Nature Methods.