متابعة
Tobias Marschall
عنوان
عدد مرات الاقتباسات
عدد مرات الاقتباسات
السنة
The complete sequence of a human genome‏
S Nurk, S Koren, A Rhie, M Rautiainen, AV Bzikadze, A Mikheenko, ...‏
Science 376 (6588), 44-53, 2022‏
26452022
Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome‏
AM Wenger, P Peluso, WJ Rowell, PC Chang, RJ Hall, GT Concepcion, ...‏
Nature biotechnology 37 (10), 1155-1162, 2019‏
15672019
Eleven grand challenges in single-cell data science‏
D Lähnemann, J Köster, E Szczurek, DJ McCarthy, SC Hicks, ...‏
Genome biology 21, 1-35, 2020‏
11872020
Multi-platform discovery of haplotype-resolved structural variation in human genomes‏
MJP Chaisson, AD Sanders, X Zhao, A Malhotra, D Porubsky, T Rausch, ...‏
Nature communications 10 (1), 1784, 2019‏
8512019
Whole-genome sequence variation, population structure and demographic history of the Dutch population‏
TG the Netherlands Consortium‏
Nature Genetics 46, 818-825, 2014‏
748*2014
High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios‏
M Byrska-Bishop, US Evani, X Zhao, AO Basile, HJ Abel, AA Regier, ...‏
Cell 185 (18), 3426-3440. e19, 2022‏
6952022
A draft human pangenome reference‏
WW Liao, M Asri, J Ebler, D Doerr, M Haukness, G Hickey, S Lu, JK Lucas, ...‏
Nature 617 (7960), 312-324, 2023‏
6642023
Haplotype-resolved diverse human genomes and integrated analysis of structural variation‏
P Ebert, PA Audano, Q Zhu, B Rodriguez-Martin, D Porubsky, MJ Bonder, ...‏
Science 372 (6537), eabf7117, 2021‏
5712021
Nanopore sequencing and the Shasta toolkit enable efficient de novo assembly of eleven human genomes‏
K Shafin, T Pesout, R Lorig-Roach, M Haukness, HE Olsen, C Bosworth, ...‏
Nature biotechnology 38 (9), 1044-1053, 2020‏
5212020
Genome-wide patterns and properties of de novo mutations in humans‏
LC Francioli, PP Polak, A Koren, A Menelaou, S Chun, I Renkens, ...‏
Nature Genetics 47 (7), 822-826, 2015‏
4262015
Mapping and phasing of structural variation in patient genomes using nanopore sequencing‏
M Cretu Stancu, MJ Van Roosmalen, I Renkens, MM Nieboer, ...‏
Nature communications 8 (1), 1326, 2017‏
4102017
WhatsHap: weighted haplotype assembly for future-generation sequencing reads‏
M Patterson, T Marschall, N Pisanti, L Van Iersel, L Stougie, GW Klau, ...‏
Journal of Computational Biology 22 (6), 498-509, 2015‏
4042015
Computational pan-genomics: status, promises and challenges‏
T Marschall, M Marz, T Abeel, L Dijkstra, BE Dutilh, A Ghaffaari, P Kersey, ...‏
Briefings in Bioinformatics, 2016‏
397*2016
A robust benchmark for detection of germline large deletions and insertions‏
JM Zook, NF Hansen, ND Olson, L Chapman, JC Mullikin, C Xiao, ...‏
Nature biotechnology 38 (11), 1347-1355, 2020‏
390*2020
The Human Pangenome Project: a global resource to map genomic diversity‏
T Wang, L Antonacci-Fulton, K Howe, HA Lawson, JK Lucas, AM Phillippy, ...‏
Nature 604 (7906), 437-446, 2022‏
3652022
WhatsHap: fast and accurate read-based phasing‏
M Martin, M Patterson, S Garg, S O Fischer, N Pisanti, GW Klau, ...‏
BioRxiv, 085050, 2016‏
3412016
Pangenome graphs‏
JM Eizenga, AM Novak, JA Sibbesen, S Heumos, A Ghaffaari, G Hickey, ...‏
Annual review of genomics and human genetics 21 (1), 139-162, 2020‏
2582020
Deep sequencing reveals differential expression of microRNAs in favorable versus unfavorable neuroblastoma‏
JH Schulte, T Marschall, M Martin, P Rosenstiel, P Mestdagh, S Schlierf, ...‏
Nucleic acids research 38 (17), 5919-5928, 2010‏
2322010
GraphAligner: rapid and versatile sequence-to-graph alignment‏
M Rautiainen, T Marschall‏
Genome biology 21 (1), 253, 2020‏
2032020
Chromosome-scale, haplotype-resolved assembly of human genomes‏
S Garg, A Fungtammasan, A Carroll, M Chou, A Schmitt, X Zhou, S Mac, ...‏
Nature Biotechnology, 1-4, 2020‏
1832020
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مقالات 1–20