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High-throughput method for the hybridisation-based targeted enrichment of long genomic fragments for PacBio third-generation sequencing.
Steiert TA, Fuß J, Juzenas S, Wittig M, Hoeppner MP, Vollstedt M, Varkalaite G, ElAbd H, Brockmann C, Görg S, Gassner C, Forster M, Franke A. Steiert TA, et al. Among authors: forster m. NAR Genom Bioinform. 2022 Jul 13;4(3):lqac051. doi: 10.1093/nargab/lqac051. eCollection 2022 Sep. NAR Genom Bioinform. 2022. PMID: 35855323 Free PMC article.
From next-generation sequencing alignments to accurate comparison and validation of single-nucleotide variants: the pibase software.
Forster M, Forster P, Elsharawy A, Hemmrich G, Kreck B, Wittig M, Thomsen I, Stade B, Barann M, Ellinghaus D, Petersen BS, May S, Melum E, Schilhabel MB, Keller A, Schreiber S, Rosenstiel P, Franke A. Forster M, et al. Among authors: forster p. Nucleic Acids Res. 2013 Jan 7;41(1):e16. doi: 10.1093/nar/gks836. Epub 2012 Sep 10. Nucleic Acids Res. 2013. PMID: 22965131 Free PMC article.
Development of a high-resolution NGS-based HLA-typing and analysis pipeline.
Wittig M, Anmarkrud JA, Kässens JC, Koch S, Forster M, Ellinghaus E, Hov JR, Sauer S, Schimmler M, Ziemann M, Görg S, Jacob F, Karlsen TH, Franke A. Wittig M, et al. Among authors: forster m. Nucleic Acids Res. 2015 Jun 23;43(11):e70. doi: 10.1093/nar/gkv184. Epub 2015 Mar 9. Nucleic Acids Res. 2015. PMID: 25753671 Free PMC article.
Two Prevalent ∼100-kb GYPB Deletions Causative of the GPB-Deficient Blood Group MNS Phenotype S-s-U- in Black Africans.
Gassner C, Denomme GA, Portmann C, Bensing KM, Mattle-Greminger MP, Meyer S, Trost N, Song YL, Engström C, Jungbauer C, Just B, Storry JR, Forster M, Franke A, Frey BM. Gassner C, et al. Among authors: forster m. Transfus Med Hemother. 2020 Jul;47(4):326-336. doi: 10.1159/000504946. Epub 2020 Jan 21. Transfus Med Hemother. 2020. PMID: 32884505 Free PMC article.
1,036 results