ArticleMethods in molecular biology (Clifton, N.J.)2025
Identification of Single Nucleotide Polymorphism from Insect Genomic Data.
Article in Methods in molecular biology (Clifton, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Molecular Identification ofInsects · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Single nucleotide polymorphisms (SNPs) are the most common type of genetic variation among individuals. SNPs are widely used to estimate genomic divergence, population structure, and natural selection, as well as to identify associations between genomic variants and phenotypic traits. However, the identification of SNPs in non-model species or from field-derived samples may still be challenging and would benefit from standardized protocols. The identification of SNPs from raw sequencing data, such as those obtained from a standard Illumina library, involves many processing steps and the use of diverse sets of tools, where the choice of different parameters significantly affects the results. Here, we present a pipeline for a genome-wide identification of SNPs from raw Illumina reads. This pipeline is composed of three major steps that encompass the GATK Best Practices and include quality control of the raw reads, mapping of short reads to a reference genome, recalibration of the alignment, variant calling, quality control for variant calling, and filtering of candidate SNPs. The steps of this pipeline are accompanied by publicly available scripts and datasets used for the identification of SNPs in the genome of the mosquito Aedes aegypti, an invasive species and a major arboviral vector worldwide.
Indexed as
Identifiers
40828273What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.