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Journal of Integrative Bioinformatics|July 27, 2011
Data partitioning enables the use of standard SOAP Web Services in genome-scale workflowsPawel Sztromwasser, Pål Puntervoll, Kjell Petersen
Plos One|July 16, 2020
Impact of processing method on donated human breast milk microRNA contentUrszula Smyczynska, Marcin A Bartlomiejczyk, Marcin M Stanczak, et al.
Bioinformatics (Oxford, England)|August 5, 2022
DBFE: distribution-based feature extraction from structural variants in whole-genome dataMaciej Piernik, Dariusz Brzezinski, Pawel Sztromwasser, et al.
Molecular Diagnosis & Therapy|December 21, 2021
Validation of HER2 Status in Whole Genome Sequencing Data of Breast Cancers with the Ploidy-Corrected Copy Number ApproachMarzena Wojtaszewska, Rafał Stępień, Alicja Woźna, et al.
Bioinformatics (Oxford, England)|June 12, 2016
RareVariantVis: new tool for visualization of causative variants in rare monogenic disorders using whole genome sequencing dataTomasz Stokowy, Mateusz Garbulowski, Torunn Fiskerstrand, et al.
American Journal of Ophthalmology|January 31, 2015
High myopia-excavated optic disc anomaly associated with a frameshift mutation in the MYC-binding protein 2 gene (MYCBP2)Cecilie Bredrup, Stefan Johansson, Laurence A Bindoff, et al.
EMBO Molecular Medicine|December 25, 2015
Defective PITRM1 mitochondrial peptidase is associated with Aβ amyloidotic neurodegenerationDario Brunetti, Janniche Torsvik, Cristina Dallabona, et al.
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