Population Genomics and Structure Analysis (PGSA01) https://prstats.org/course/population-genomics-and-structure-analysis-pgsa01/ Live Online Course (28 September–2 October 2026 Working with SNP, RAD-seq, whole-genome, low-coverage, or ancient DNA datasets? Looking …

Population Genomics and Structure Analysis (PGSA01) https://prstats.org/course/population-genomics-and-structure-analysis-pgsa01/ Delivered by Dr. Nikolay Oskolkov, a computational biologist and bioinformatician with expertise in population genomics, evolutionary biology, machine …

Hi- I have 133 strains of L. plantarum strain sequences (from NCBI database), and for my work, I want to double check that these are …

Hi, A professor asked me to design primers for the detection of *Pseudomonas* spp.. The idea is to detect *Pseudomonas* reads in cancer samples. According …

<p>Hi All,</p> <p>What is the best and current bioinformatics approach to assign functions to putative/hypothetical proteins?</p> <p>Thanks</p>

<p>Hi,</p> <p>I have many VCF files (each for different bacteria spp.) for SNPs/INDELs that I just want to extract SNPs/INDELs from. Then I will like …

Hi, I am working with whole genome sequences of bacteria and want to identify SNPs from the genomes for each sequences. What would be the …

<p>HI,</p> <p>I have created a data-set f non-homologous protein sequences from PDB in order to study certain secondary structures. After that, I obtained a list …

<p>Hi,</p> <p>Is it a good idea to concatenate contigs for doing comparative genome analysis? Any suggestions for the correct approach will be appreciated.</p> <p>Thanks</p>

<p>Hi fellows,</p> <p>I'm now looking for the variants files from a published CELL paper entitled "Evolutionary History and Adaptation from High-Coverage Whole-Genome Sequences of Diverse …