A Practical Introduction to NGS Data Analysis and Variant Calling
Do you work with sequencing...
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FINAL CALL - A Practical Introduction to NGS Data Analysis and Variant Calling (Munich, Germany | September 9–11, 2026)
Munich, Germany | September 9–11, 2026
A Practical Introduction to NGS Data Analysis and Variant Calling
Do you work with sequencing... -
Searching for databases and repositories for AML rna seq data
I am looking Rna seq data of AML patients. i have tried GDC portal and i only found data on only around 300 patients can someone suggest other databases... -
Alignment to multiple reference sequences
Hello,
I'm interested in determining if plasmid sequences are in a NGS data set and I was thinking about creating a master fasta file with... -
Concrodance NGS and array genotypes
Hi SEQanswers folks,
for Sample based QC we would like to calculate the concordance of NGS genotypes from a VCF file and Illumina Array...Last edited by genomixer; 10-15-2015, 07:39 AM. -
Webinar: How to Integrate Microarray & NGS Data
Microarray and Next-Generation Sequencing don’t have to live in separate worlds. In this webinar you will learn to:
*Combine microarray... -
computational tools for STR discovery
Hi,
I am looking for tools available for discovering STR's from NGS datasets. So far I have come up with lobSTR. Does anyone have information... -
NGS Diagnostics: Annotation and Interpretation
NGS Diagnostics: Annotation and Interpretation
August 19-20, 2015 | Capital Hilton Hotel, Washington, DC
http://www.nextgenerationdx.co... -
Whicn normalization methods are used for RNAseqv2 data at TCGA?
Hi,
I have downloaded the RNAseqV2 data for BRCA. there are diffrent version of expression values inside of the RNAseqV2, Level 3 folder.... -
Cuffdiff problem output!!!
i have some problem related to cuffidiff output, i used this command for replicates:
cuffdiff -o diff_out -b <genome.fa> -p 10 -L CT,SS...Last edited by ALOK N PATEL; 11-27-2013, 03:49 AM. -
Is it normal to have NGS paired read data to be complementary?
Hi,
I am new to NGS data analysis. I have got NGS read data from the Demo run. The Data is from HLA typing using NGS Technology. On looking... -
Next Generation Sequencing Data Summit
Oxford Global's Next Generation Sequencing Data Congress taking place on the 17th & 18th June 2013 in London. The Congress is focused on the current...Last edited by Oxford_Global_DPatel; 02-13-2013, 12:34 AM. -
The Next Generation Sequencing Data Congress -17th & 18th June 2013, London
As part of our key NGS series of events - Oxford Global Conferences are proud to present The Next Generation Sequencing Data Congress.
Over...Last edited by daniellemeredith; 02-13-2013, 08:47 AM. -
Normalization of small RNA data for library size
Hi,
I have a few libraries of small RNA reads with different read counts: some libraries have more than 10 million reads, some others have <1... -
Where can I find FASTQ files along with reference genomes for various species?
Please could anyone direct me to sources (ftp or otherwise) where I could find a number of FASTQ files pertaining to various organisms along with the...
