I'll be attending the coveted Marco Island meeting early next month (February 4 - 8), where I'll present a poster on my evaluations of short read aligners for next -
gen sequencing data.
Conceptually, SNVs should be the easiest things to find in next -
gen sequencing data.
Yet those who produce next -
gen sequencing data are rapidly adopting this universal short read data format as the de facto standard.
With longer (> 50 bp) fragment - end reads and / or paired - end libraries, it's possible to detect small insertion / deletion variants (indels) in next -
gen sequencing data.
Not exact matches
The job will entail working on a team of 20 software engineers on next -
gen sequence analysis pipelines, focusing on utilizing the information management capabilities of the analysis system to migrate
data appropriately between different tiers of storage and eliminate
data duplication.