Stanislav Volik

According to our database, Stanislav Volik authored at least 6 papers between 2003 and 2024.

Collaborative distances:

• Dijkstra number of four.
• Erdős number of three.

2024

Phenotype prediction from single-cell RNA-seq data using attention-based neural networks.

Yuzhen Mao, Yen-Yi Lin, Nelson K. Y. Wong, Stanislav Volik, Funda Sar, Colin C. Collins, Martin Ester

Bioinform., February, 2024

2019

Alignment-free clustering of UMI tagged DNA molecules.

Baraa Orabi, Emre Erhan, Brian McConeghy, Stanislav V. Volik, Stephane Le Bihan, Robert Bell, Colin C. Collins, Cédric Chauve, Faraz Hach

Bioinform., 2019

2017

SiNVICT: ultra-sensitive detection of single nucleotide variants and indels in circulating tumour DNA.

Can Kockan, Faraz Hach, Iman Sarrafi, Robert H. Bell, Brian McConeghy, Kevin Beja, Anne Haegert, Alexander W. Wyatt, Stanislav Volik, Kim N. Chi, Colin C. Collins, Süleyman Cenk Sahinalp

Bioinform., 2017

2011

Comrad: detection of expressed rearrangements by integrated analysis of RNA-Seq and low coverage genome sequence data.

Andrew W. McPherson, Chunxiao Wu, Iman Hajirasouliha, Fereydoun Hormozdiari, Faraz Hach, Anna Lapuk, Stanislav Volik, Sohrab P. Shah, Colin C. Collins, Süleyman Cenk Sahinalp

Bioinform., 2011

2008

Evaluation of Paired-End Sequencing Strategies for Detection of Genome Rearrangements in Cancer.

Ali Bashir, Stanislav Volik, Colin C. Collins, Vineet Bafna, Benjamin J. Raphael

PLoS Comput. Biol., 2008

2003

Reconstructing tumor genome architectures.

Benjamin J. Raphael, Stanislav Volik, Colin C. Collins, Pavel A. Pevzner

Proceedings of the European Conference on Computational Biology (ECCB 2003), 2003