Event box
Analyzing NGS Data: Standard data processing and workflow analysis on high powered computing environment In-Person
The NGS technologies have the potential to dramatically accelerate biomedical research by enabling
comprehensive analysis of genomes and transcriptomes to become inexpensive, routine, and
widespread tools. This workshop will focus on methods for base‐calling and variant‐calling, for aligning
reads to reference sequences (e.g. genomes), and for de novo assembly of short reads into longer
sequences. The following tools will be covered on a shared research cluster; quality reports
of FASTQ files, trimming and filtering of reads, alignment and coverage objects such as SAM/BAM files
using bowtie/bwa, calling SNPs with Samtools, and De novo Assembly using Velvet.
- Date:
- Thursday, January 23, 2020
- Time:
- 2:00pm - 5:00pm
- Time Zone:
- Eastern Time - US & Canada (change)
- Location:
- Countway L2: Room 025
- Categories:
- Bioinformatics
Event Organizer
I am available for individual consultations with the Harvard community. Please consult my calendar via the link below, and reserve a time which is most convenient for you.
Scott's Consultation Appointment Schedule
Thanks!
-Scott