Webinar on Unique Molecular Identifier (UMI)-powered Ultra-sensitive Variant Calling using Strand NGS on 13 Dec at 2:30 PM and 9:30 PM IST by Dr.Pandurang Kolekar

Unique Molecular Identifiers (UMIs) are short random nucleotide sequences that are increasingly being used in high-throughput sequencing experiments. In this webinar, we will highlight the UMI-friendly features of Strand NGS v3.1 including support for handling well known and customised UMI libraries, QC metrics, consensus alignment, UMI-based family size filters for read list, genome browser enabled … Continue reading “Webinar on Unique Molecular Identifier (UMI)-powered Ultra-sensitive Variant Calling using Strand NGS on 13 Dec at 2:30 PM and 9:30 PM IST by Dr.Pandurang Kolekar”

Configuring SNP detection pipelines for accurate analysis of clinical samples

Webinar of the Month Series: Configuring SNP detection pipelines in Avadis NGS for accurate analysis of clinical samples Presenter:  Dr Vamsi Veeramachaneni, Vice President, Strand Life Sciences Abstract: Running a SNP detection pipeline and identifying high quality variant calls quickly is challenging. This is especially true in the case of clinical labs where multiple panels … Continue reading “Configuring SNP detection pipelines for accurate analysis of clinical samples”