#  Analyzing NGS Data: Standard data processing and workflow analysis on high powered computing environment 

 



####  calendar\_today Date and Time 

 **November 28, 2018** 

 10:00AM - 01:00PM EST 

####  pin\_drop Location 

 **Countway Floor L2: 025**  



 

 



 

 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 Orchestra, 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.

 Register [here](https://libcal.library.harvard.edu/event/4665149)



 

 



 

 See also:- [ All Graduate Students ](/audience/all-graduate-students)
- [ Academic and Professional Skills ](/resource/academic-and-professional-skills)
- [ Quantitative and Computational Skills ](/resource/quantitative-and-computational-skills)
- [ Harvard Provider ](/provider/harvard-provider)
 
 

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