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Evin M. Padhi

dblp:305/6347 · DBLP profile ↗
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2ranked-venue papers
1as first author
2since 2021 · last 2026
0000-0003-2578-2435ORCID · corroborated

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 2 · 1 first-author · 2 since 2021

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
2 papers
Bioinformatics and computational biology · 100%

Topics — the 6 heaviest of 6, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
genomics
1.012026
Genomics-informed approach identifies which cell types regulate the metabolome · Bioinform. 2026
Bioinformatics and computational biology
single-cell analysis
1.012026
Genomics-informed approach identifies which cell types regulate the metabolome · Bioinform. 2026
Bioinformatics and computational biology
comparative genomics
0.512021
ACES: Analysis of Conservation with an Extensive list of Species · Bioinform. 2021
Bioinformatics and computational biology
phylogenetics
0.512021
ACES: Analysis of Conservation with an Extensive list of Species · Bioinform. 2021
Bioinformatics and computational biology › phylogenetics
phylogenetic inference
0.512021
ACES: Analysis of Conservation with an Extensive list of Species · Bioinform. 2021
Bioinformatics and computational biology › sequence analysis › sequence comparison
sequence conservation analysis
0.512021
ACES: Analysis of Conservation with an Extensive list of Species · Bioinform. 2021

Methods — techniques the papers use, named apart from their topics

single-cell RNA sequencing integration · 1.0genome-wide association · 1.0multiple sequence alignment · 0.5BLAST · 0.5
YearPublicationVenuePosition
2026 Genomics-informed approach identifies which cell types regulate the metabolome
abstract
MOTIVATION: Metabolism occurs in a cell type-specific manner, but which cells regulate metabolite levels remains unclear. RESULTS: Here, we integrate some of the largest metabolite quantitative trait loci datasets, TOPMed and UK Biobank, with one of the most extensive single-cell RNA sequencing resources, Tabula Sapiens. This integration allows us to identify cell types that regulate metabolites body-wide. We find hepatocytes are the primary regulatory cell type for most metabolites, associating with 385/410 (94%) metabolites for whom an association is found. Additionally, our multi-gene approach reveals more metabolite associations with beta cells compared to those identified using a single-gene approach. For example, we identify novel metabolite-cell type associations, such as the association between phenylpropanoic acid and beta cells, this metabolite that was previously thought to be regulated by the microbiome. AVAILABILITY: Code used in this work is available via Github at https://github.com/haimkru/Metabolite-Cell-Type-Associations.
Haim Krupkin, Evin M. Padhi, Daniel Nachun, Jessica Kain, Jonathan Z. Long, Stephen B. Montgomery
Bioinform.2
2021 ACES: Analysis of Conservation with an Extensive list of Species
abstract
MOTIVATION: An abundance of new reference genomes is becoming available through large-scale sequencing efforts. While the reference FASTA for each genome is available, there is currently no automated mechanism to query a specific sequence across all new reference genomes. RESULTS: We developed ACES (Analysis of Conservation with an Extensive list of Species) as a computational workflow to query specific sequences of interest (e.g. enhancers, promoters, exons) against reference genomes with an available reference FASTA. This automated workflow generates BLAST hits against each of the reference genomes, a multiple sequence alignment file, a graphical fragment assembly file and a phylogenetic tree file. These data files can then be used by the researcher in several ways to provide key insights into conservation of the query sequence. AVAILABILITY AND IMPLEMENTATION: ACES is available at https://github.com/TNTurnerLab/ACES. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Evin M. Padhi, Jeffrey K. Ng, Elvisa Mehinovic, Eleanor I Sams, Tychele Turner
Bioinform.1