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HELLO: improved neural network architectures and methodologies for small variant calling., , , and . BMC Bioinform., 22 (1): 404 (2021)A recurrent Markov state-space generative model for sequences., , , and . AISTATS, volume 89 of Proceedings of Machine Learning Research, page 3070-3079. PMLR, (2019)Recommendations for performance optimizations when using GATK3.8 and GATK4., , , , , , , , , and 5 other author(s). BMC Bioinform., 20 (1): 557:1-557:9 (2019)LeafCutterMD: an algorithm for outlier splicing detection in rare diseases., , , , , and . Bioinform., 36 (17): 4609-4615 (2020)AMOD: a morpholino oligonucleotide selection tool., , , , and . Nucleic Acids Res., 33 (Web-Server-Issue): 506-511 (2005)Deep Phenotyping of Non-Alcoholic Fatty Liver Disease Patients with Genetic Factors for Insights into the Complex Disease., , , , , , , and . CoRR, (2023)Proceedings of the 15th Annual UT-KBRIN Bioinformatics Summit 2016: Cadiz, KY, USA. 8-10 April 2016., , , , , , , , , and 70 other author(s). BMC Bioinform., (August 2016)A supervised learning method for classifying methylation disorders., , , , , , , , , and 3 other author(s). BMC Bioinform., 25 (1): 66 (December 2024)Deep Learning for Better Variant Calling for Cancer Diagnosis and Treatment., , , , and . ASP-DAC, page 16-21. IEEE, (2018)Genie: an MPEG-G conformant software to compress genomic data, , , , , , , , , and 15 other author(s). International Conference for High Performance Computing, Networking, Storage and Analysis (SC19), page (poster). (November 2019)