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Michael Stromberg
Michael Stromberg
Illumina
Verified email at bc.edu
Title
Cited by
Cited by
Year
A map of human genome variation from population scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
87172010
Mapping copy number variation by population-scale genome sequencing
RE Mills, K Walter, C Stewart, RE Handsaker, K Chen, C Alkan, A Abyzov, ...
Nature 470 (7332), 59-65, 2011
12672011
BamTools: a C++ API and toolkit for analyzing and managing BAM files
DW Barnett, EK Garrison, AR Quinlan, MP Strömberg, GT Marth
Bioinformatics 27 (12), 1691-1692, 2011
8832011
Demographic history and rare allele sharing among human populations
S Gravel, BM Henn, RN Gutenkunst, AR Indap, GT Marth, AG Clark, F Yu, ...
Proceedings of the National Academy of Sciences 108 (29), 11983-11988, 2011
7072011
Whole-genome sequencing and variant discovery in C. elegans
LDW Hillier, GT Marth, AR Quinlan, D Dooling, G Fewell, D Barnett, P Fox, ...
Nature methods 5 (2), 183-188, 2008
5832008
Rapid whole-genome mutational profiling using next-generation sequencing technologies
DR Smith, AR Quinlan, HE Peckham, K Makowsky, W Tao, B Woolf, ...
Genome research 18 (10), 1638-1642, 2008
3592008
Isaac: ultra-fast whole-genome secondary analysis on Illumina sequencing platforms
C Raczy, R Petrovski, CT Saunders, I Chorny, S Kruglyak, EH Margulies, ...
Bioinformatics 29 (16), 2041-2043, 2013
3492013
MOSAIK: a hash-based algorithm for accurate next-generation sequencing short-read mapping
WP Lee, MP Stromberg, A Ward, C Stewart, EP Garrison, GT Marth
PloS one 9 (3), e90581, 2014
3462014
Pyrobayes: an improved base caller for SNP discovery in pyrosequences
AR Quinlan, DA Stewart, MP Strömberg, GT Marth
Nature methods 5 (2), 179-181, 2008
3332008
A comprehensive map of mobile element insertion polymorphisms in humans
C Stewart, D Kural, MP Strömberg, JA Walker, MK Konkel, AM Stütz, ...
PLoS genetics 7 (8), e1002236, 2011
3242011
Pisces: an accurate and versatile variant caller for somatic and germline next-generation sequencing data
T Dunn, G Berry, D Emig-Agius, Y Jiang, S Lei, A Iyer, N Udar, ...
Bioinformatics 35 (9), 1579-1581, 2019
632019
Expression divergence measured by transcriptome sequencing of four yeast species
MA Busby, JM Gray, AM Costa, C Stewart, MP Stromberg, D Barnett, ...
BMC genomics 12, 1-15, 2011
332011
SNP discovery using advanced algorithms and neural networks
P Unneberg, M Strömberg, F Sterky
Bioinformatics 21 (10), 2528-2530, 2005
182005
Analysis of 70,000 EST sequences to study divergence between two closely related Populus species
P Unneberg, M Strömberg, J Lundeberg, S Jansson, F Sterky
Tree genetics & genomes 1, 109-115, 2005
152005
Image classification using the frequencies of simple features
CS Lindsey, M Strömberg
Pattern Recognition Letters 21 (3), 265-268, 2000
102000
Nirvana: clinical grade variant annotator
M Stromberg, R Roy, J Lajugie, Y Jiang, H Li, E Margulies
Proceedings of the 8th ACM International Conference on Bioinformatics …, 2017
72017
MOSAIK read alignment and assembly program
M Strömberg, WP Lee
72009
Pisces: An accurate and versatile single sample somatic and germline variant caller
T Dunn, G Berry, D Emig-Agius, Y Jiang, A Iyer, N Udar, M Strömberg
Proceedings of the 8th ACM International Conference on Bioinformatics …, 2017
22017
Enabling high-throughput sequencing data analysis with MOSAIK
MP Stromberg
Boston College, 2010
22010
MOSAIK: A hash-based algorithm for accurate next-generation sequencing read mapping
WP Lee, M Stromberg, A Ward, C Stewart, E Garrison, GT Marth
genetics 20, 2869-78, 0
1
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