Genomic Signatures of Selection Are Enriched in Differentially Expressed Genes in Sticklebacks Adapting to Contrasting Environments.
Paper
Loaded from Europe PMC by your browser, not stored by OSCR: doi.org · Europe PMC
The paper is loaded when this pane is shown.
The authors' code
Perl · 36 lines · 869 B · no license
- #!/usr/bin/perl
- my $usage= "
- Prints out list of commands for launcher_creator.py
- to bowtie2-map the trimmed 36b 2bRAD reads
- Arguments:
- 1: glob to fastq files
- 2: reference to map to (basename of bowtie2 index file)
- 3: optional, the position of name-deriving string in the file name
- if separated by underscores,
- such as: input file Sample_RNA_2DVH_L002_R1.cat.fastq
- specifying arg2 as \'3\' would create output file with a name \'2DVH.fastq'
- ";
- if (!$ARGV[0]) { die $usage;}
- my $glob=$ARGV[0];
- if (!$ARGV[1]) { die $usage;}
- my $ref=$ARGV[1];
- opendir THIS, ".";
- my @fqs=grep /$glob/,readdir THIS;
- my $outname="";
- foreach $fqf (@fqs) {
- if ($ARGV[2]) {
- my @parts=split('_',$fqf);
- $outname=$parts[$ARGV[1]-1].".bt2.sam";
- }
- else { $outname=$fqf.".bt2.sam";}
- print "bowtie2 --no-unal --score-min L,16,1 --local -L 16 -x $ref -U $fqf -S $outname\n";
- }
2bRAD_bowtie2_launch.pl at commit 0c8a25f, no license · at the source
Overview
- Department of Ecology and Evolution, Stony Brook University, Stony Brook, NY 11794, USA
- The Graduate Program in Genetics, Stony Brook University, Stony Brook, NY 11794, USA
- Department of Molecular Genetics and Microbiology, Duke University, Durham, NC 27710, USA
- University Program in Genetics and Genomics, Duke University, Durham, NC 27710, USA
- Department of Biology, The College of New Jersey, Ewing, NJ 08628, USA
Abstract
Whole genome scans have identified numerous adaptive alleles in many species; however, linking these alleles to specific phenotypes remains a major challenge. A promising alternative to direct genotype–phenotype mapping, particularly given the complexities introduced by epistasis, pleiotropy, and environmental variability, is to assess whether differentially expressed genes (DEGs) are enriched in regions of genetic divergence between populations adapted to contrasting environments. Here, we study gene expression patterns in threespine stickleback populations adapting to contrasting environments (marine vs. freshwater) and investigate signatures of selection associated with gene expression evolution during adaptation. We performed transcriptomic experiments of the brain and gill tissues of wild-caught sticklebacks sampled from one marine and two freshwater environments using TagSeq. We found that DEGs in the freshwater environments harbor single nucleotide polymorphisms (SNPs) previously identified to be involved in rapid adaptation and FST outliers. A majority of these SNPs were located in cis-regulatory regions of the genes with predicted low to moderate effects on protein function and structure, although we found a high-impact SNP in the gene col8a1b. Genes such as pvalb4 and acsl4a, involved in calcium regulation in the gill and fatty acid metabolism in the brain, respectively, were enriched with SNPs showing signatures of selection. By linking signatures of selection to tissue-specific gene expression patterns, our study bridges the gap between genomic divergence and the molecular mechanisms underlying physiological adaptation to new environments and identifies specific pathways that can be targeted for future functional studies.
Reproduced under the paper's license (CC BY), from the paper cited above.
Repository
Its files are read in the Code ↔ Paper reader above.
z0on/tag-based_RNAseq
0c8a25f81e7c0d35ef9c527d1f5a060db9c96b1f, 11 January 2021Availability: 1 check, the latest on 26 September 2026: the link answers
- 26 September 2026: the link answers
30 files
- 2bRAD_bowtie2_launch.pl, Perl, 36 lines
- countreads.pl, Perl, 21 lines
- dna.mixing.R, R, 49 lines
- dupCount.R, R, 27 lines
- expression_compiler.pl, Perl, 47 lines
- heatmapEveryWhichWay.R, R, 132 lines
- iRNAseq_shrimpmap_SAM.pl
, Perl, 42 lines - iRNAseq_trim_launch0.pl, Perl, 34 lines
- isogroup_namer.pl, Perl, 67 lines
- launcher_creator.py, Python, 536 lines
- ls5_launcher_creator.py, Python, 460 lines
- mix_illumina_qpcr.R, R, 66 lines
- ngs_concat.pl, Perl, 41 lines
- picogreen.R, R, 30 lines
- rnaseq_clipper0.pl, Perl, 60 lines
- rnaseq_clipper_fasta.pl, Perl, 50 lines
- rnaseq_clipper_old.pl, Perl, 59 lines
- samcount.pl, Perl, 134 lines
- samcount_launch.pl, Perl, 34 lines
- samcount_launch_bt2.pl, Perl, 25 lines
- samcount_v.0.1.pl, Perl, 143 lines
- selectFastaByHeader.pl, Perl, 38 lines
- splitFastaByHeader.pl, Perl, 48 lines
- tagseq_bowtie2map.pl, Perl, 42 lines
- tagseq_clipper.pl, Perl, 96 lines
- tagseq_trim_launch.pl, Perl, 42 lines
- tagseq_trim_launch_bgi.p
l , Perl, 31 lines - thetaByContig.py, Python, 148 lines
- uniHeatmap.R, R, 89 lines
- README.md, Text, 24 lines
The paper's code and data availability statement is in the Data section.
Tracing map
Proposed by the machine: these links were found in the paper and verified at the source, without human review. The map will receive a Zenodo DOI once one of the paper's authors has validated it with their ORCID.
What the map holds:
- 1 repository of the authors' code, each at its verified commit, with its license and how the link was found in the paper;
- 29 scripts, each with its path and the digest of its content;
- no match between paragraphs and code yet;
- neither the text of the paper nor the code itself.
Its JSON (tracing-map.json) is deposited on Zenodo with its DOI once the map is validated.
Data
Data links
- ncbi.nlm.nih.gov/
sra , NCBI; found in “Data Availability”
Data Availability
All sequenced raw reads have been deposited on Sequence Read Archive (www.ncbi.nlm.nih.gov/
Reproduced under the paper's license (CC BY), from the paper cited above.
Versions
The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.
Version 1, 27 September 2026: the first record
Recorded: type, language, journal, volume, issue, pages, dates, 4 authors, 5 keywords, 8 MeSH terms, 1 funder, 120 references.
Cite
This paper
Kwakye, A., Dzikowski, N., Wund, M. A., & Veeramah, K. R. (2026). Genomic Signatures of Selection Are Enriched in Differentially Expressed Genes in Sticklebacks Adapting to Contrasting Environments. Genome biology and evolution, 18(9), evag222. https://
BibTeX
@article{kwakye2026genom
author = {Kwakye, Alexander and Dzikowski, Natalie and Wund, Matthew A and Veeramah, Krishna R},
title = {{Genomic Signatures of Selection Are Enriched in Differentially Expressed Genes in Sticklebacks Adapting to Contrasting Environments}},
journal = {Genome biology and evolution},
year = {2026},
month = sep,
volume = {18},
number = {9},
pages = {evag222},
publisher = {Oxford University Press},
issn = {1759-6653},
doi = {10.1093/
url = {https://
pmid = {42668140},
pmcid = {PMC13583502}
}
RIS
TY - JOUR
AU - Kwakye, Alexander
AU - Dzikowski, Natalie
AU - Wund, Matthew A
AU - Veeramah, Krishna R
TI - Genomic Signatures of Selection Are Enriched in Differentially Expressed Genes in Sticklebacks Adapting to Contrasting Environments
T2 - Genome biology and evolution
J2 - Genome Biol Evol
PY - 2026
DA - 2026/
VL - 18
IS - 9
SP - evag222
SN - 1759-6653
PB - Oxford University Press
DO - 10.1093/
UR - https://
LA - en
ER -
CSL-JSON
{
"id": "10.1093/
"type": "article-journal",
"title": "Genomic Signatures of Selection Are Enriched in Differentially Expressed Genes in Sticklebacks Adapting to Contrasting Environments",
"container-title": "Genome biology and evolution",
"author": [
{
"family": "Kwakye",
"given": "Alexander"
},
{
"family": "Dzikowski",
"given": "Natalie"
},
{
"family": "Wund",
"given": "Matthew A"
},
{
"family": "Veeramah",
"given": "Krishna R"
}
],
"container-title-short":
"volume": "18",
"issue": "9",
"page": "evag222",
"DOI": "10.1093/
"PMID": "42668140",
"PMCID": "PMC13583502",
"ISSN": "1759-6653",
"publisher": "Oxford University Press",
"URL": "https://
"language": "en",
"issued": {
"date-parts": [
[
2026,
9,
1
]
]
}
}
The tracing map gets a citation of its own once an author has validated it and it has a DOI.
Similar papers
The papers with a page that share the most with this one: the tools found in their code, their categories, datasets, cited references and authors, the rarest counting most.
- [1] doi:10.1093/molbev/msag149 [code]
- Multiple modes of selection underlie repeated and human-mediated adaptation in a formerly migratory fish.Journal: Molecular biology and evolutionIn common: NumPy, other, cellular / molecular, 6 references
- [2] doi:10.1093/bioinformatics/btag592 [code]
- Network-based stratification of allele-specific expression reveals patient subgroups in Huntington's disease.Journal: Bioinformatics (Oxford, England)In common: pheatmap, NumPy, genetics / omics, 4 references
- [3] doi:10.1038/s41586-026-10391-0 [code]
- Cell-type-targeted mitochondrial transplantation rescues cell degeneration.Journal: NatureIn common: NumPy, cellular / molecular, 5 references
- [4] doi:10.3390/biology15131038 [code]
- Genetic Basis of Divergent Growth and Muscle Development in Purebred and Crossbred Leizhou Black Goats Revealed by Whole-Genome Resequencing.Journal: BiologyIn common: other, genetics / omics, cellular / molecular, 3 references
- [5] doi:10.1242/jcs.264529
- Increased Glycine-N-methyltransfer
ase expression disrupts light-dependent gene expression rhythms in the Drosophila eye. Journal: Journal of cell scienceIn common: cellular / molecular, 4 references - [6] doi:10.1038/s41467-026-72598-z [code]
- Functional impact of genetic background on variable expressivity in neurodevelopmental disorders.Journal: Nature communicationsIn common: pheatmap, NumPy, 3 references
- [7] doi:10.1016/j.cell.2026.05.026 [code]
- The critical role of the endogenous immune compartment after CAR T cell therapy in recurrent GBM.Journal: CellIn common: NumPy, genetics / omics, 4 references
- [8] doi:10.1038/s41586-026-10629-x [code]
- Whole-genome duplication shaped cell-type evolution in the vertebrate brain.Journal: NatureIn common: pheatmap, NumPy, other, genetics / omics, cellular / molecular, 2 references
- [9] doi:10.1038/s41467-026-76675-1 [code]
- Long-read proteogenomic atlas of human neuronal differentiation reveals isoform diversity informing neurodevelopmental risk mechanisms.Journal: Nature communicationsIn common: pheatmap, NumPy, genetics / omics, 3 references
- [10] doi:10.21203/rs.3.rs-9927928/v1 [code]
- Genome-wide and allele-resolved maps of the radial architecture of the mouse genomeJournal: Research Square (preprint)In common: pheatmap, NumPy, genetics / omics, 3 references
Contribute
The authors of this paper can claim it, correct its record and validate its tracing map, and the maintainers of its code (its owner, or a public member of its organization) correct what it says of their repository; anyone signed in can ask for its removal. Every request goes to OSCR's own machine, which answers it; your account page follows them.
Sign in with ORCID to claim this paper as one of its authors, correct its record or validate its tracing map: when the paper's metadata lists your ORCID iD, you are recognized at once. Maintainers of its code: sign in with GitHub, then claim the repository on your account page.
Claim this paper
Correct its record
Say what each link of this record is, remove the ones that are not the paper's, add the ones that are missing. The correction becomes a new version of the record, in its Versions section.
Validate its tracing map
You validate the map as this page shows it: 1 repository of the authors' code, each at its verified commit and with its license, 29 scripts, and 0 matches between paragraphs and code (see the Code and Map sections). It then receives a DOI on Zenodo, with you (your ORCID iD) and OSCR as its creators; the code itself is not deposited.
The map's fingerprint: sha256:1ca381d992b89468…
Add the badge to its README
The badge links the code to this page. Copy one of these into the README of the paper's code: only you decide where it goes, and nothing is changed for you.
Markdown
[, paste the snippet at the top, then “Commit changes…” and, to review it first, “Create a new branch and start a pull request”. You open the pull request; OSCR asks for no permission.
Request its removal
To ask OSCR to remove this record, the copies of its authors' scripts or its tracing map, use the removal request page: signed in, you say who you are, what to remove and why, then review and confirm the request. Published rules decide every request (how).
Discussion, reproductions, activity
Discussion: questions and error reports about this paper and its code, from signed-in readers and its authors. It opens with sign-in.
Reproductions: reports from readers who ran the authors' code: what they reproduced, with which environment, commit and data. It opens with sign-in.
Activity: what happens around this paper: new versions of its record, its map's validation, discussions and reproductions. It opens with sign-in.
