by Stuart Davis | Jul 6, 2022 | Announcements
As you may already know, Basepair offers a number of very popular tools for ChIP-seq analysis, seamlessly taking your FASTQ files to meaningful results. From trimming and alignment, peak calling and annotation, to motif enrichment and now, pathway enrichment analysis...
by Amit | Mar 26, 2022 | Announcements
Writers write, painters paint, genomics researchers… wait patiently for algorithm pipelines to finish processing NGS data, only to spend as much time visualizing results? As long-time researchers and bioinformaticians, we’re well aware that in NGS data analysis, every...
by Stuart Davis | Mar 18, 2022 | Announcements
With a large number of companies and universities taking extensive measures to curb the spread of COVID-19, many employees are now working remotely. A range of software tools help remote teams seamlessly manage messages, meetings, and projects. Slack for messaging,...
by Stuart Davis | Feb 6, 2022 | Announcements
FASTQ files. Except they’re not “just” files, not “just” data. They’re the culmination of countless hours of running experiments, library preparation, sequencing, etc. You spent all this time gathering data — probably more time than you would have liked — so by the...
by Amit | May 7, 2021 | Announcements
When auditing goes wrong Is your genomics team keeping track of the open source tools it’s using? What about software version numbers and the parameters being set? Genome reference files, usage logs, the custom scripts bioinformaticians are deploying? If you’re not...
by Stuart Davis | Dec 4, 2020 | Announcements
If you ask the Basepair team what makes them excited to work at Basepair, they’d probably say that it’s the knowledge that they’re creating solutions that make research faster and accessible for more scientists. But what makes the team especially excited is when they...
