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Author Details
Full Name
Faraz Hach
Affiliation
University of British Columbia
ORCID
Career Start Year
1999
Papers
38
H Index
17
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36895072
Differentiation of Peritubular Myoid-Like Cells from Human Induced Pluripotent Stem Cells.
Adv Biol (Weinh)
2023
36546757
Optimized high-throughput screening of non-coding variants identified from genome-wide association studies.
Nucleic Acids Res
2023
35164688
Genion, an accurate tool to detect gene fusion from long transcriptomics reads.
BMC Genomics
2022
35747387
Fast and accurate matching of cellular barcodes across short-reads and long-reads of single-cell RNA-seq experiments.
iScience
2022
36071171
Genetic determinants of chromatin reveal prostate cancer risk mediated by context-dependent gene regulation.
Nat Genet
2022
35303886
Fast characterization of segmental duplication structure in multiple genome assemblies.
Algorithms Mol Biol
2022
33975627
Functional mapping of androgen receptor enhancer activity.
Genome Biol
2021
33532821
Detecting high-scoring local alignments in pangenome graphs.
Bioinformatics
2021
34489572
An androgen receptor switch underlies lineage infidelity in treatment-resistant prostate cancer.
Nat Cell Biol
2021
32259207
CircMiner: accurate and rapid detection of circular RNA through splice-aware pseudo-alignment scheme.
Bioinformatics
2020
32029828
Identification of gene signature for treatment response to guide precision oncology in clear-cell renal cell carcinoma.
Sci Rep
2020
32781410
HASLR: Fast Hybrid Assembly of Long Reads.
iScience
2020
30561550
lordFAST: sensitive and Fast Alignment Search Tool for LOng noisy Read sequencing Data.
Bioinformatics
2019
30351359
Alignment-free clustering of UMI tagged DNA molecules.
Bioinformatics
2019
29267878
Computational identification of micro-structural variations and their proteogenomic consequences in cancer.
Bioinformatics
2018
30011247
Dynamic Alignment-Free and Reference-Free Read Compression.
J Comput Biol
2018
30423092
Fast characterization of segmental duplications in genome assemblies.
Bioinformatics
2018
27531099
SiNVICT: ultra-sensitive detection of single nucleotide variants and indels in circulating tumour DNA.
Bioinformatics
2017
28954787
Mutational Analysis of Gene Fusions Predicts Novel MHC Class I-Restricted T-Cell Epitopes and Immune Signatures in a Subset of Prostate Cancer.
Clin Cancer Res
2017
28881988
Discovery and genotyping of novel sequence insertions in many sequenced individuals.
Bioinformatics
2017
27776113
Comparison of high-throughput sequencing data compression tools.
Nat Methods
2016
27587673
CoLoRMap: Correcting Long Reads by Mapping short reads.
Bioinformatics
2016
25461772
Fast and accurate mapping of Complete Genomics reads.
Methods
2015
26382624
Robustness of Massively Parallel Sequencing Platforms.
PLoS One
2015
26005866
Spatial genomic heterogeneity within localized, multifocal prostate cancer.
Nat Genet
2015
24130305
ORMAN: optimal resolution of ambiguous RNA-Seq multimappings in the presence of novel isoforms.
Bioinformatics
2014
25357237
DeeZ: reference-based compression by local assembly.
Nat Methods
2014
24810850
mrsFAST-Ultra: a compact, SNP-aware mapper for high performance sequencing applications.
Nucleic Acids Res
2014
22294438
Integrated genome and transcriptome sequencing identifies a novel form of hybrid and aggressive prostate cancer.
J Pathol
2012
23047557
SCALCE: boosting sequence compression algorithms using locally consistent encoding.
Bioinformatics
2012
22689759
Dissect: detection and characterization of novel structural alterations in transcribed sequences.
Bioinformatics
2012
22553170
From sequence to molecular pathology, and a mechanism driving the neuroendocrine phenotype in prostate cancer.
J Pathol
2012
21131385
Alu repeat discovery and characterization within human genomes.
Genome Res
2011
21586516
Sensitive and fast mapping of di-base encoded reads.
Bioinformatics
2011
21478487
Comrad: detection of expressed rearrangements by integrated analysis of RNA-Seq and low coverage genome sequence data.
Bioinformatics
2011
20676076
mrsFAST: a cache-oblivious algorithm for short-read mapping.
Nat Methods
2010
20529927
Next-generation VariationHunter: combinatorial algorithms for transposon insertion discovery.
Bioinformatics
2010
10912111
[Family physician Dr. Friedrich Hach. Hospitals save--we pay the difference. Interview by Werner Loosen].
MMW Fortschr Med
1999
1 - 38 of 38
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