Live webinar on DNA-Seq Data Analysis - Selected Case Studies on 22 Feb 2017

Strandlife · 01-31-2017, 09:48 PM

Webinar on DNA-Seq data analysis- Case Studies

DNA-Seq data can be analyzed and visualized using an extensive workflow in Strand NGS software. The software has been designed for the biologists. Strand NGS supports analysis of whole exome, whole genome and targeted sequencing experiments. The DNA-Seq workflow includes the ability to detect variants (SNPs, MNPs and short InDels), annotate them with dbSNP, and report for each SNP the kind of effect it has on the genes and provides list of affected genes. Biological contextualization of the affected genes can be performed by downstream analysis such as GO, GSA, pathway analysis.

Large structural variations, including large insertions, deletions, inversions, and translocations, can also be detected with paired-end and mate-paired data. Copy number variation (CNV) analysis can be done using tumor-normal pairs. Strand NGS has easy to use built in pipelines (with an option to customize) for time consuming jobs which automates analysis and leaves more time for end data interpretation. In this webinar we will discuss case studies using the DNA-Seq data analysis workflow in Strand NGS and also highlight on parameters within each feature that can be optimized depending on datasets and analysis needs.

Details:
Session 1: 2:30 PM IST, 22 Feb
Session 2: 10:30 PM IST, 22 Feb

Speaker: Dr. Suman Kapoor, Manager- Application Science at Strand Life Sciences, has over 10 years experience in molecular biology, next-generation sequencing based testing, clinical genomics, and personalized medicine for disease management and prenatal testing. Dr. Suman holds a Ph.D in Molecular and Cell Biology from Indian Institute of Science, Bangalore. Prior to joining Strand NGS team, Suman has worked extensively on protein synthesis in eubacteria and has experience working in CAP and NABL accredited lab validating and interpreting NGS based diagnostic tests.

Register here: http://www.strand-ngs.com/webinar_registration

Strandlife · 02-20-2017, 11:50 PM

Just a day to go for our webinar on DNA-Seq Data Analysis in StrandNGS. Hurry! Register at http://www.strand-ngs.com/webinar_registration

Strandlife · 05-16-2017, 02:43 AM

In case you missed the webinar, because of your busy schedule, you can access the recording here http://www.strand-ngs.com/learn/webinar-recordings

Strandlife · 07-26-2017, 05:10 AM

Excited to learn about prediction methods using statistical workflows? Register to the upcoming webinar by Dr Mario Deng, Professor of Medicine, UCLA and learn the application of NGS and Machine learning to predict post-operative recovery of advanced heart failure patients.
Details: 9 Aug 2017, 8 am PST. Register at http://www.strand-ngs.com/webinar_registration

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01-31-2017, 09:48 PM	#1
Strandlife strandlife Location: All over the world Join Date: May 2013 Posts: 67	Live webinar on DNA-Seq Data Analysis - Selected Case Studies on 22 Feb 2017 Webinar on DNA-Seq data analysis- Case Studies DNA-Seq data can be analyzed and visualized using an extensive workflow in Strand NGS software. The software has been designed for the biologists. Strand NGS supports analysis of whole exome, whole genome and targeted sequencing experiments. The DNA-Seq workflow includes the ability to detect variants (SNPs, MNPs and short InDels), annotate them with dbSNP, and report for each SNP the kind of effect it has on the genes and provides list of affected genes. Biological contextualization of the affected genes can be performed by downstream analysis such as GO, GSA, pathway analysis. Large structural variations, including large insertions, deletions, inversions, and translocations, can also be detected with paired-end and mate-paired data. Copy number variation (CNV) analysis can be done using tumor-normal pairs. Strand NGS has easy to use built in pipelines (with an option to customize) for time consuming jobs which automates analysis and leaves more time for end data interpretation. In this webinar we will discuss case studies using the DNA-Seq data analysis workflow in Strand NGS and also highlight on parameters within each feature that can be optimized depending on datasets and analysis needs. Details: Session 1: 2:30 PM IST, 22 Feb Session 2: 10:30 PM IST, 22 Feb Speaker: Dr. Suman Kapoor, Manager- Application Science at Strand Life Sciences, has over 10 years experience in molecular biology, next-generation sequencing based testing, clinical genomics, and personalized medicine for disease management and prenatal testing. Dr. Suman holds a Ph.D in Molecular and Cell Biology from Indian Institute of Science, Bangalore. Prior to joining Strand NGS team, Suman has worked extensively on protein synthesis in eubacteria and has experience working in CAP and NABL accredited lab validating and interpreting NGS based diagnostic tests. Register here: http://www.strand-ngs.com/webinar_registration Last edited by Strandlife; 01-31-2017 at 09:49 PM. Reason: Spelling correction

02-20-2017, 11:50 PM	#2
Strandlife strandlife Location: All over the world Join Date: May 2013 Posts: 67	Just a day to go for our webinar on DNA-Seq Data Analysis in StrandNGS. Hurry! Register at http://www.strand-ngs.com/webinar_registration

05-16-2017, 02:43 AM	#3
Strandlife strandlife Location: All over the world Join Date: May 2013 Posts: 67	In case you missed the webinar, because of your busy schedule, you can access the recording here http://www.strand-ngs.com/learn/webinar-recordings

07-26-2017, 05:10 AM	#4
Strandlife strandlife Location: All over the world Join Date: May 2013 Posts: 67	Excited to learn about prediction methods using statistical workflows? Register to the upcoming webinar by Dr Mario Deng, Professor of Medicine, UCLA and learn the application of NGS and Machine learning to predict post-operative recovery of advanced heart failure patients. Details: 9 Aug 2017, 8 am PST. Register at http://www.strand-ngs.com/webinar_registration