Single-cell RNA Sequencing to Elucidate Tumor and Tumor Subclone-Specific Cancer Phenotypes

por Marth, Gabor
Publicado en J Biomol Tech (2020)

EagleView: A genome assembly viewer for next-generation sequencing technologies

por Huang, Weichun, Marth, Gabor
Publicado 2008

ped_draw: pedigree drawing with ease

por Velinder, Matt, Lee, Dillon, Marth, Gabor
Publicado en BMC Bioinformatics (2020)

Toolbox for Mobile-Element Insertion Detection on Cancer Genomes

por Lee, Wan-Ping, Wu, Jiantao, Marth, Gabor T
Publicado en Cancer Inform (2014)

Toolbox for Mobile-Element Insertion Detection on Cancer Genomes

por Lee, Wan-Ping, Wu, Jiantao, Marth, Gabor T
Publicado en Cancer Inform (2015)

2254: iobio: From academic project to commercial enterprise

por Ward, Alistair N., Miller, Chase, Marth, Gabor
Publicado en J Clin Transl Sci (2018)

The allele frequency spectrum in genome-wide human variation data reveals signals of differential demographic history in three large world populations.

por Marth, Gabor T, Czabarka, Eva, Murvai, Janos, Sherry, Stephen T
Publicado 2004

ART: a next-generation sequencing read simulator

por Huang, Weichun, Li, Leping, Myers, Jason R., Marth, Gabor T.
Publicado 2012

Scribl: an HTML5 Canvas-based graphics library for visualizing genomic data over the web

por Miller, Chase A., Anthony, Jon, Meyer, Michelle M., Marth, Gabor
Publicado 2013

SSW Library: An SIMD Smith-Waterman C/C++ Library for Use in Genomic Applications

por Zhao, Mengyao, Lee, Wan-Ping, Garrison, Erik P., Marth, Gabor T.
Publicado 2013

Analysis of concordance of different haplotype block partitioning algorithms

por Indap, Amit R, Marth, Gabor T, Struble, Craig A, Tonellato, Peter, Olivier, Michael
Publicado 2005

Variant discovery in targeted resequencing using whole genome amplified DNA

por Indap, Amit R, Cole, Regina, Runge, Christina L, Marth, Gabor T, Olivier, Michael
Publicado 2013

STRP Screening Sets for the human genome at 5 cM density

por Ghebranious, Nader, Vaske, David, Yu, Adong, Zhao, Chengfeng, Marth, Gabor, Weber, James L
Publicado 2003

Human Diallelic Insertion/Deletion Polymorphisms

por Weber, James L., David, Donna, Heil, Jeremy, Fan, Ying, Zhao, Chengfeng, Marth, Gabor
Publicado 2002

Scotty: a web tool for designing RNA-Seq experiments to measure differential gene expression

por Busby, Michele A., Stewart, Chip, Miller, Chase A., Grzeda, Krzysztof R., Marth, Gabor T.
Publicado 2013

bam.iobio: a web-based, real-time, sequence alignment file inspector

por Miller, Chase A, Qiao, Yi, DiSera, Tonya, D’Astous, Brian, Marth, Gabor T
Publicado en Nat Methods (2014)

Sequence Assembly with CAFTOOLS

por Dear, Simon, Durbin, Richard, Hillier, LaDeana, Marth, Gabor, Thierry-Mieg, Jean, Mott, Richard
Publicado 1998

BamTools: a C++ API and toolkit for analyzing and managing BAM files

por Barnett, Derek W., Garrison, Erik K., Quinlan, Aaron R., Strömberg, Michael P., Marth, Gabor T.
Publicado 2011

MOSAIK: A Hash-Based Algorithm for Accurate Next-Generation Sequencing Short-Read Mapping

por Lee, Wan-Ping, Stromberg, Michael P., Ward, Alistair, Stewart, Chip, Garrison, Erik P., Marth, Gabor T.
Publicado 2014

GIGGLE: a search engine for large-scale integrated genome analysis

por Layer, Ryan M, Pedersen, Brent S, DiSera, Tonya, Marth, Gabor T, Gertz, Jason, Quinlan, Aaron R
Publicado en Nat Methods (2018)