12 citations · 19 across the 4 of their papers we have counts for
4 papers
A frame-based representation of genomic sequences for removing errors and rare variant detection in NGS data
Raunaq Malhotra, Manjari Mukhopadhyay, Mary Poss +1
We propose a frame-based representation of k-mers for detecting sequencing errors and rare variants in next generation sequencing data obtained from populations of closely related…
Maximum Likelihood de novo reconstruction of viral populations using paired end sequencing data
Raunaq Malhotra, Manjari Mukhopadhyay Steven Wu, Allen Rodrigo +2
We present MLEHaplo, a maximum likelihood de novo assembly algorithm for reconstructing viral haplotypes in a virus population from paired-end next generation sequencing (NGS) data…
Clustering pipeline for determining consensus sequences in targeted next-generation sequencing
Raunaq Malhotra, Daniel Elleder, Le Bao +3
Analyses of targeted genomic sequencing data from next-generation-sequencing (NGS) technologies typically involves mapping reads to a reference sequence or clustering reads. For a…
On Breaching Enterprise Data Privacy Through Adversarial Information Fusion
Srivatsava Ranjit Ganta, Raj Acharya
Data privacy is one of the key challenges faced by enterprises today. Anonymization techniques address this problem by sanitizing sensitive data such that individual privacy is pre…