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A Genomic Data Fusion Framework to Exploit Rare and Common Variants for Association Discovery.

, , , , и . AIME, том 9105 из Lecture Notes in Computer Science, стр. 101-105. Springer, (2015)

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Constantin Romulus Ivan

Svilen Ivanov

Sarah Ivanovas

Marian Ivanov

Elizaveta Ivanova

 

Другие публикации лиц с тем же именем

A kinetic model-based algorithm to classify NGS short reads by their allele origin., , , , и . J. Biomed. Informatics, (2015)PaPI: pseudo amino acid composition to score human protein-coding variants., , и . BMC Bioinform., (2015)A Genomic Data Fusion Framework to Exploit Rare and Common Variants for Association Discovery., , , , и . AIME, том 9105 из Lecture Notes in Computer Science, стр. 101-105. Springer, (2015)A Rule-Based Expert System for Automatic Implementation of Somatic Variant Clinical Interpretation Guidelines., , , , , , и . AIME, том 11526 из Lecture Notes in Computer Science, стр. 114-119. Springer, (2019)Kimimila: A New Model to Classify NGS Short Reads by Their Allele Origin., , , , и . ICHI, стр. 340-342. IEEE Computer Society, (2014)BigQ: a NoSQL based framework to handle genomic variants in i2b2., , , , , и . BMC Bioinform., (2015)Big Data as a Driver for Clinical Decision Support Systems: A Learning Health Systems Perspective., , , , , , , , , и 2 other автор(ы). Frontiers Digit. Humanit., (2018)A Semi-supervised Learning Approach for Pan-Cancer Somatic Genomic Variant Classification., , , , , , и . AIME, том 11526 из Lecture Notes in Computer Science, стр. 42-46. Springer, (2019)