Iman Hajirasouliha
Iman Hajirasouliha
Assistant Professor, Weill Cornell Medicine of Cornell University, New York City
Email verificata su - Home page
Citata da
Citata da
A map of human genome variation from population-scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
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
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
Integrative annotation of variants from 1092 humans: application to cancer genomics
E Khurana, Y Fu, V Colonna, XJ Mu, HM Kang, T Lappalainen, A Sboner, ...
Science 342 (6154), 1235587, 2013
Next-generation VariationHunter: combinatorial algorithms for transposon insertion discovery
F Hormozdiari, I Hajirasouliha, P Dao, F Hach, D Yorukoglu, C Alkan, ...
Bioinformatics 26 (12), i350-i357, 2010
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel
O Delaneau, J Marchini, GA McVean, P Donnelly, G Lunter, JL Marchini, ...
Nature communications 5, 3934, 2014
From sequence to molecular pathology, and a mechanism driving the neuroendocrine phenotype in prostate cancer
AV Lapuk, C Wu, AW Wyatt, A McPherson, BJ McConeghy, S Brahmbhatt, ...
The Journal of pathology 227 (3), 286-297, 2012
Biomolecular network motif counting and discovery by color coding
N Alon, P Dao, I Hajirasouliha, F Hormozdiari, SC Sahinalp
Bioinformatics 24 (13), i241-i249, 2008
Detection and characterization of novel sequence insertions using paired-end next-generation sequencing
I Hajirasouliha, F Hormozdiari, C Alkan, JM Kidd, I Birol, EE Eichler, ...
Bioinformatics 26 (10), 1277-1283, 2010
Fast and scalable inference of multi-sample cancer lineages
V Popic, R Salari, I Hajirasouliha, D Kashef-Haghighi, RB West, ...
Genome biology 16 (1), 91, 2015
Alu repeat discovery and characterization within human genomes
F Hormozdiari, C Alkan, M Ventura, I Hajirasouliha, M Malig, F Hach, ...
Genome Research 21 (6), 840-849, 2011
A combinatorial approach for analyzing intra-tumor heterogeneity from high-throughput sequencing data
I Hajirasouliha, A Mahmoody, BJ Raphael
Bioinformatics 30 (12), i78-i86, 2014
Simultaneous structural variation discovery among multiple paired-end sequenced genomes
F Hormozdiari, I Hajirasouliha, A McPherson, EE Eichler, SC Sahinalp
Genome research 21 (12), 2203-2212, 2011
Deep convolutional neural networks enable discrimination of heterogeneous digital pathology images
P Khosravi, E Kazemi, M Imielinski, O Elemento, I Hajirasouliha
EBioMedicine 27, 317-328, 2018
Integrated genome and transcriptome sequencing identifies a novel form of hybrid and aggressive prostate cancer
C Wu, AW Wyatt, AV Lapuk, A McPherson, BJ McConeghy, RH Bell, ...
The Journal of Pathology, 2012
MATE-CLEVER: Mendelian-inheritance-aware discovery and genotyping of midsize and long indels
T Marschall, I Hajirasouliha, A Schnhuth
Bioinformatics 29 (24), 3143-3150, 2013
Comrad: detection of expressed rearrangements by integrated analysis of RNA-Seq and low coverage genome sequence data
A McPherson, C Wu, I Hajirasouliha, F Hormozdiari, F Hach, A Lapuk, ...
Bioinformatics 27 (11), 1481, 2011
Characterization of structural variants with single molecule and hybrid sequencing approaches
A Ritz, A Bashir, S Sindi, D Hsu, I Hajirasouliha, BJ Raphael
Bioinformatics 30 (24), 3458-3466, 2014
Deep learning enables robust assessment and selection of human blastocysts after in vitro fertilization
P Khosravi, E Kazemi, Q Zhan, JE Malmsten, M Toschi, P Zisimopoulos, ...
NPJ digital medicine 2 (1), 1-9, 2019
Il sistema al momento non pu eseguire l'operazione. Riprova pi tardi.
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