Marcel Martin
Marcel Martin
Email verificata su scilifelab.se
Titolo
Citata da
Citata da
Anno
Cutadapt removes adapter sequences from high-throughput sequencing reads
M Martin
EMBnet. journal 17 (1), pp. 10-12, 2011
94002011
Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3
M Martin, L Maßhöfer, P Temming, S Rahmann, C Metz, N Bornfeld, ...
Nature genetics 45 (8), 933, 2013
3362013
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
1972010
Computational pan-genomics: status, promises and challenges
Briefings in bioinformatics 19 (1), 118-135, 2016
1382016
A comprehensive molecular study on Coffin–Siris and Nicolaides–Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling
D Wieczorek, N Bögershausen, F Beleggia, S Steiner-Haldenstätt, E Pohl, ...
Human molecular genetics 22 (25), 5121-5135, 2013
1342013
Production of individualized V gene databases reveals high levels of immunoglobulin genetic diversity
MM Corcoran, GE Phad, NV Bernat, C Stahl-Hennig, N Sumida, ...
Nature communications 7, 13642, 2016
982016
The genetic basis for ecological adaptation of the Atlantic herring revealed by genome sequencing
AM Barrio, S Lamichhaney, G Fan, N Rafati, M Pettersson, H Zhang, ...
elife 5, e12081, 2016
952016
Cloche is a bHLH-PAS transcription factor that drives haemato-vascular specification
S Reischauer, OA Stone, A Villasenor, N Chi, SW Jin, M Martin, MT Lee, ...
Nature 535 (7611), 294-298, 2016
862016
SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population
A Ameur, J Dahlberg, P Olason, F Vezzi, R Karlsson, M Martin, J Viklund, ...
European Journal of Human Genetics 25 (11), 1253-1260, 2017
712017
Exact and heuristic algorithms for weighted cluster editing
S Rahmann, T Wittkop, J Baumbach, M Martin, A Truss, S Böcker
Computational Systems Bioinformatics: (Volume 6), 391-401, 2007
702007
Discovering motifs that induce sequencing errors
M Allhoff, A Schönhuth, M Martin, IG Costa, S Rahmann, T Marschall
BMC bioinformatics 14 (5), S1, 2013
642013
Clinical and mutation data in 12 patients with the clinical diagnosis of Nager syndrome
JC Czeschik, C Voigt, Y Alanay, B Albrecht, S Avci, D Fitzpatrick, ...
Human genetics 132 (8), 885-898, 2013
622013
Atropos: specific, sensitive, and speedy trimming of sequencing reads
JP Didion, M Martin, FS Collins
PeerJ 5, e3720, 2017
582017
Massive parallel bisulfite sequencing of CG-rich DNA fragments reveals that methylation of many X-chromosomal CpG islands in female blood DNA is incomplete
M Zeschnigk, M Martin, G Betzl, A Kalbe, C Sirsch, K Buiting, S Gross, ...
Human molecular genetics 18 (8), 1439-1448, 2009
452009
The SEQanswers wiki: a wiki database of tools for high-throughput sequencing analysis
JW Li, K Robison, M Martin, A Sjödin, B Usadel, M Young, EC Olivares, ...
Nucleic acids research 40 (D1), D1313-D1317, 2011
432011
Oto-facial syndrome and esophageal atresia, intellectual disability and zygomatic anomalies-expanding the phenotypes associated with EFTUD2 mutations
C Voigt, A Mégarbané, K Neveling, JC Czeschik, B Albrecht, B Callewaert, ...
Orphanet journal of rare diseases 8 (1), 110, 2013
392013
Amplikyzer: automated methylation analysis of amplicons from bisulfite flowgram sequencing
S Rahmann, J Beygo, D Kanber, M Martin, B Horsthemke, K Buiting
PeerJ PrePrints, 2013
312013
WhatsHap: fast and accurate read-based phasing
M Martin, M Patterson, S Garg, S Fischer, N Pisanti, GW Klau, ...
bioRxiv, 085050, 2016
302016
Next‐generation RNA sequencing reveals differential expression of MYCN target genes and suggests the mTOR pathway as a promising therapy target in MYCN‐amplified neuroblastoma
A Schramm, J Köster, T Marschall, M Martin, M Schwermer, K Fielitz, ...
International journal of cancer 132 (3), E106-E115, 2013
292013
De novo assembly of two Swedish genomes reveals missing segments from the human GRCh38 reference and improves variant calling of population-scale sequencing data
A Ameur, H Che, M Martin, I Bunikis, J Dahlberg, I Höijer, S Häggqvist, ...
Genes 9 (10), 486, 2018
272018
Il sistema al momento non può eseguire l'operazione. Riprova più tardi.
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