scispace - formally typeset
V

Vladimir Semenyuk

Publications -  11
Citations -  351

Vladimir Semenyuk is an academic researcher. The author has contributed to research in topics: Genome & Reference genome. The author has an hindex of 6, co-authored 10 publications receiving 233 citations.

Papers
More filters
Journal ArticleDOI

Fast and accurate genomic analyses using genome graphs.

TL;DR: The Graph Genome Pipeline as discussed by the authors is a graph reference genome implementation that enables read alignment across 2,800 diploid genomes encompassing 12.6 million SNPs and 4.0 million insertions and deletions (indels).
Posted ContentDOI

precisionFDA Truth Challenge V2: Calling variants from short- and long-reads in difficult-to-map regions

Nathan D. Olson, +75 more
- 15 Nov 2020 - 
TL;DR: The precisionFDA Truth Challenge V2 aimed to assess the state-of-the-art of variant calling in difficult-to-map regions and the Major Histocompatibility Complex and new methods out-performed the 2016 Truth Challenge winners.
Patent

Method and apparatus for coding information

TL;DR: In this article, a method and apparatus for coding information that is specifically adapted for smaller presentation formats, such as in a hand held video player, is presented, inter alia, reducing the complexity of video decoding, implementation of an MP3 decoder using fixed point arithmetic, fast YcbCr to RGB conversion, encapsulation of a video stream and an MP 3 audio stream into an AVI file, storing menu navigation and DVD subpicture information on a memory card, synchronization of audio and video streams, encryption of keys that are used for decryption of multimedia data, and
Posted ContentDOI

Fast and Accurate Genomic Analyses using Genome Graphs

TL;DR: This work presents a graph genome implementation that enables read alignment across 2,800 diploid genomes encompassing 12.6 million SNPs and 4.0 million indels and shows that iterative augmentation of graph genomes yields incremental gains in variant calling accuracy.
Patent

Systems and methods for genomic pattern analysis

TL;DR: In this article, the authors propose a method for analyzing sequence data in which a large amount and variety of reference data are efficiently modeled as a reference graph, such as a directed acyclic graph (DAG).