Sameer Paithankar

ClinGen Pathogenicity Calculator: a configurable system for assessing pathogenicity of genetic variants

Shawn Rynearson, Heidi L. Rehm, Aleksandar Milosavljevic, 2017, Genome Medicine.

An integrative variant analysis suite for whole exome next-generation sequencing data

Aleksandar Milosavljevic, Cristian Coarfa, Fuli Yu, 2012, BMC Bioinformatics.

Analysis of interactions between the epigenome and structural mutability of the genome using Genboree workbench tools

Adrian V. Lee, Andrew R. Jackson, A. Milosavljevic, 2014, BMC Bioinformatics.

Epigenomic footprints across 111 reference epigenomes reveal tissue-specific epigenetic regulation of lincRNAs

Andrew R. Jackson, A. Milosavljevic, C. Coarfa, 2015, Nature Communications.

ClinGen Allele Registry links information about genetic variants

Aleksandar Milosavljevic, Piotr Pawliczek, Chris Bizon, 2018, Human mutation.

Atlas2 Cloud: a framework for personal genome analysis in the cloud

Uday S. Evani, Andrew R. Jackson, A. Milosavljevic, 2012, BMC Genomics.

Enabling Atlas2 personal genome analysis on the cloud

Aleksandar Milosavljevic, Cristian Coarfa, Matthew N. Bainbridge, 2011, 2011 IEEE International Workshop on Genomic Signal Processing and Statistics (GENSIPS).

The Genboree Microbiome Toolset and the analysis of 16S rRNA microbial sequences

Jun Ma, Maria Diaz, Aleksandar Milosavljevic, 2012, BMC Bioinformatics.

Tetracycline treatment targeting Wolbachia affects expression of an array of proteins in Brugia malayi parasite

S. Vedi, A. Dube, Sameer Paithankar, 2009, Proteomics.

Atlas2 Cloud: a framework for personal genome analysis in the cloud

Aleksandar Milosavljevic, Cristian Coarfa, Fuli Yu, 2012, BMC Genomics.

Analysis of interactions between the epigenome and structural mutability of the genome using Genboree workbench tools

Aleksandar Milosavljevic, Viren Amin, Cristian Coarfa, 2014, BMC Bioinformatics.