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researcher

R. Acharya

4 papers hereh-index 9294 citations58 works total

Matching runs newest-first, so older work may not be attached to this profile yet.

author position
  • middle author1
  • last author3

Across the 4 of 4 papers where every author was matched, so the position is known.

fields
  • q-bio.GN2
  • cs.DB1
  • q-bio.PE1
same name
  • R. Acharya — 27 papers, h 23
  • R. Acharya — 12 papers, h 7
  • R. Acharya — 10 papers, h 9
  • R. Acharya — 6 papers, h 7
  • R. Acharya — 2 papers, h 5
  • R. Acharya — 2 papers, h 2

Either other researchers who publish under this name, or the same person where the external sources have not merged their records.

identity via Semantic Scholar / OpenAlex

activity
20082016
most citedMaximum Likelihood de novo reconstruction of viral populations using paired end sequencing data

12 citations · 19 across the 4 of their papers we have counts for

collaborators
Showing q-bio.GNShow all

2 papers · 1 filter

q-bio.GN2016★ 2 cited

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…

q-bio.GN2014★ 5 cited

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…

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Not affiliated with arXiv. Researcher data from Semantic Scholar (ODC-BY) and OpenAlex.