Vladimir Makarov

Abstract 2230: Low frequency variant detection in cell free DNA by applying molecular identifiers to targeted NGS

Ashley Wood, Sukhinder K. Sandhu, Mida Pezeshkian, 2018 .

Use of in vitro OmniPlex libraries for high-throughput comparative genomics and molecular haplotyping

Vladimir Makarov, Emmanuel Kamberov, Irina Sleptsova, 2002, SPIE BiOS.

Software review Computer programs for eukaryotic gene prediction

Vladimir Makarov, 2002 .

Meta-analysis of gene expression for development and validation of a diagnostic biomarker panel for Oral Squamous Cell Carcinoma

Vladimir Makarov, Alex Gorlin, V. Makarov, 2019, Comput. Biol. Chem..

Analysis of Rare, Exonic Variation amongst Subjects with Autism Spectrum Disorders and Population Controls

Kathryn Roeder, Stephan Ripke, Shannon Gross, 2013, PLoS genetics.

Family-based association tests for sequence data, and comparisons with population-based association tests

Iuliana Ionita-Laza, Seunggeun Lee, Vladimir Makarov, 2013, European Journal of Human Genetics.

Consortium, G.P A map of human genome variation from population-scale sequencing. Nature 467, 1061-1073

Ken Chen, Joshua M. Korn, Afidalina Tumian, 2010 .

Two methods of whole-genome amplification enable accurate genotyping across a 2320-SNP linkage panel.

Vladimir Makarov, Roger S Lasken, Irina Sleptsova, 2004, Genome research.