Ceske Budejovice, Czech Republic, See here for full event details and apply online
This workshop covers microbiomics / metagenomics analysis...
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Genomic Medicine 2018 Nordic Workshop & Conference
The fifth annual GENOMIC MEDICINE 2018 NORDIC Conference & Workshop will take place at the South Denmark University (SDU) in Odense on 2nd & 3rd...
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NGS Data Analysis Workshop & Genomic Symposium in Nijmegen
GENOMIC MEDICINE 2018 NIJMEGEN WORKSHOP will take place on 9th October at Concertgebouw de Vereeniging.
This NGS Data Analysis Workshop will...
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Are you new to NGS and don't know where to start? - Introduction to NGS
Check out our 'Introduction to NGS Data Analysis' course in Berlin. The target audience is biologists or data analysts with no or little experience in...
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FeatureCounts highest counts for unstranded option
Dear All,
I am working on RNASeq data which is generated using Truseq straded HT kit.
I have done removing adapters and...
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FeatureCounts highest counts for unstranded option
Dear All,
I am working on RNASeq data which is generated using Truseq straded HT kit.
I have done removing adapters and...
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DeNovo Assembly and Variant Calling Data Analysis Workshop, Oct 8-12, 2018, Prague
4th Prague Autumn School, Prague, Czech Republic, See here for full event details and apply online
After three successful years we are...
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Bioinformatics/Data analysis - Washington University - $52,769 - $71,240
Please apply at: https://jobs.wustl.edu/
Job ID 37913
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[email protected] started a topic Analyzing Cell-Free DNA Seq Data from Cancer Patients to find Actionable Variantsin EpigeneticsAnalyzing Cell-Free DNA Seq Data from Cancer Patients to find Actionable Variants
Webinar:
How to Analyze Cell-Free DNA Sequencing Data from Cancer Patients to Identify Clinically Actionable Variants
In this webinar,...
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Genomic Medicine 2017 Cambridge
The Genomic Medicine 2017 Cambridge meeting on 26th & 27th September will cover areas where Next Generation Sequencing is used in the analysis of...
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[ddRAD] on removal of duplicate reads
Hi All,
Is it advisable to remove duplicate reads from double digest RAD (ddRAD) data generated on Illumina Hiseq platform ?
...
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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....
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pR2 function fails on fully populated R object
Hi,
The R package, pscl, is meant for statistical analysis. The pR2 function that calculates "pseudo R-sq" has been failing with...
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Postdoctoral researchers (Cancer Genomics) at Memorial Sloan Kettering Cancer Center
We are seeking two motivated postdoctoral researchers to join our lab at Memorial Sloan Kettering Cancer Center in New York City. Our lab specializes...