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Author Details
Full Name
Can Alkan
Affiliation
Bilkent University
ORCID
Career Start Year
2001
Papers
95
H Index
48
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36685727
BLEND: a fast, memory-efficient and accurate mechanism to find fuzzy seed matches in genome analysis.
NAR Genom Bioinform
2023
37018152
Identification of protein-protein interaction bridges for multiple sclerosis.
Bioinformatics
2023
35303886
Fast characterization of segmental duplication structure in multiple genome assemblies.
Algorithms Mol Biol
2022
35697522
Polishing copy number variant calls on exome sequencing data via deep learning.
Genome Res
2022
36516232
CONGA: Copy number variation genotyping in ancient genomes and low-coverage sequencing data.
PLoS Comput Biol
2022
35962045
Author Correction: Comparative and demographic analysis of orang-utan genomes.
Nature
2022
35976109
FastRemap: a tool for quickly remapping reads between genome assemblies.
Bioinformatics
2022
33315064
SneakySnake: a fast and accurate universal genome pre-alignment filter for CPUs, GPUs and FPGAs.
Bioinformatics
2021
34446078
Technology dictates algorithms: recent developments in read alignment.
Genome Biol
2021
32192518
VALOR2: characterization of large-scale structural variants using linked-reads.
Genome Biol
2020
32699374
Author Correction: A robust benchmark for detection of germline large deletions and insertions.
Nat Biotechnol
2020
32541955
A robust benchmark for detection of germline large deletions and insertions.
Nat Biotechnol
2020
29617724
Nanopore sequencing technology and tools for genome assembly: computational analysis of the current state, bottlenecks and future directions.
Brief Bioinform
2019
31496881
Characterizing microsatellite polymorphisms using assembly-based and mapping-based tools.
Turk J Biol
2019
30923804
Shouji: a fast and efficient pre-alignment filter for sequence alignment.
Bioinformatics
2019
30937433
Discovery of tandem and interspersed segmental duplications using high-throughput sequencing.
Bioinformatics
2019
29764378
GRIM-Filter: Fast seed location filtering in DNA read mapping using processing-in-memory technologies.
BMC Genomics
2018
30076130
Realizing the potential of blockchain technologies in genomics.
Genome Res
2018
30124947
Hercules: a profile HMM-based hybrid error correction algorithm for long reads.
Nucleic Acids Res
2018
30039363
Whole-Genome Shotgun Sequence CNV Detection Using Read Depth.
Methods Mol Biol
2018
30983868
Evaluation of genome scaffolding tools using pooled clone sequencing.
Turk J Biol
2018
30423092
Fast characterization of segmental duplications in genome assemblies.
Bioinformatics
2018
29391599
Targeting PLK1 overcomes T-DM1 resistance via CDK1-dependent phosphorylation and inactivation of Bcl-2/xL in HER2-positive breast cancer.
Oncogene
2018
28073353
Discovery of large genomic inversions using long range information.
BMC Genomics
2017
28881988
Discovery and genotyping of novel sequence insertions in many sequenced individuals.
Bioinformatics
2017
28583483
Toolkit for automated and rapid discovery of structural variants.
Methods
2017
28575161
GateKeeper: a new hardware architecture for accelerating pre-alignment in DNA short read mapping.
Bioinformatics
2017
26943675
Demographically-Based Evaluation of Genomic Regions under Selection in Domestic Dogs.
PLoS Genet
2016
26568624
Optimal seed solver: optimizing seed selection in read mapping.
Bioinformatics
2016
27419916
Inter-varietal structural variation in grapevine genomes.
Plant J
2016
27153582
On genomic repeats and reproducibility.
Bioinformatics
2016
25586472
Activating mutations of STAT5B and STAT3 in lymphomas derived from γδ-T or NK cells.
Nat Commun
2015
26382624
Robustness of Massively Parallel Sequencing Platforms.
PLoS One
2015
26432246
An integrated map of structural variation in 2,504 human genomes.
Nature
2015
26553077
Determining the origin of synchronous multifocal bladder cancer by exome sequencing.
BMC Cancer
2015
25461772
Fast and accurate mapping of Complete Genomics reads.
Methods
2015
25577434
Shifted Hamming distance: a fast and accurate SIMD-friendly filter to accelerate alignment verification in read mapping.
Bioinformatics
2015
24418700
Reconstructing complex regions of genomes using long-read sequencing technology.
Genome Res
2014
25385592
Comparative analysis of the domestic cat genome reveals genetic signatures underlying feline biology and domestication.
Proc Natl Acad Sci U S A
2014
25376095
Whole genome sequencing of Turkish genomes reveals functional private alleles and impact of genetic interactions with Europe, Asia and Africa.
BMC Genomics
2014
25143822
Annotated features of domestic cat - Felis catus genome.
Gigascience
2014
24810850
mrsFAST-Ultra: a compact, SNP-aware mapper for high performance sequencing applications.
Nucleic Acids Res
2014
24764354
Early postzygotic mutations contribute to de novo variation in a healthy monozygotic twin pair.
J Med Genet
2014
24453982
Genome sequencing highlights the dynamic early history of dogs.
PLoS Genet
2014
23375656
Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorder.
Am J Hum Genet
2013
23884656
Rates and patterns of great ape retrotransposition.
Proc Natl Acad Sci U S A
2013
23823723
Great ape genetic diversity and population history.
Nature
2013
23721540
The genome sequencing of an albino Western lowland gorilla reveals inbreeding in the wild.
BMC Genomics
2013
23369189
Accelerating read mapping with FastHASH.
BMC Genomics
2013
22398555
Insights into hominid evolution from the gorilla genome sequence.
Nature
2012
1 - 50 of 95
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