
Ever been sitting at your computer wondering if your sample sequencing results are ones that you want to cheer about or ones that require a dreaded redo? One of the greatest challenges in NGS analysis is finding easily interpretable answers to common bioinformatic questions, like how to assess sample quality.
Illumina has an informatics blog at https://blog.software.illumina.com/. The blog already includes information about Dragen, a high-speed data analysis system, and information about performing spatial analysis using BaseSpace. BaseSpace can help you to quickly assess and analyze data, regardless of whether you have a background in bioinformatics. Plus, posts containing information on how to access and download multiomic demo datasets are coming soon!
If you or one of your collaborators are interested in learning how to determine if a run looks good you should check out this recent post : https://blog.software.illumina.com/2021/06/14/basespace-sequence-hub-does-my-sequencing-run-look-good/. It’s dedicated to walking users through data quality analyses using the Base Space sequencing data analysis tool.
Ever been sitting at your computer wondering if your sample sequencing results are ones that you want to cheer about or ones that require a dreaded redo? One of the greatest challenges in NGS analysis is finding easily interpretable answers to common bioinformatic questions, like how to assess sample quality.
Illumina has an informatics blog at https://blog.software.illumina.com/. The blog already includes information about Dragen, a high-speed data analysis system, and information about performing spatial analysis using BaseSpace. BaseSpace can help you to quickly assess and analyze data, regardless of whether you have a background in bioinformatics. Plus, posts containing information on how to access and download multiomic demo datasets are coming soon!
If you or one of your collaborators are interested in learning how to determine if a run looks good you should check out this recent post : https://blog.software.illumina.com/2021/06/14/basespace-sequence-hub-does-my-sequencing-run-look-good/. It’s dedicated to walking users through data quality analyses using the Base Space sequencing data analysis tool.
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Ever been sitting at your computer wondering if your sample sequencing results are ones that you want to cheer about or ones that require a dreaded redo? One of the greatest challenges in NGS analysis is finding easily interpretable answers to common bioinformatic questions, like how to assess sample quality.
Illumina has an informatics blog at https://blog.software.illumina.com/. The blog already includes information about Dragen, a high-speed data analysis system, and information about performing spatial analysis using BaseSpace. BaseSpace can help you to quickly assess and analyze data, regardless of whether you have a background in bioinformatics. Plus, posts containing information on how to access and download multiomic demo datasets are coming soon!
If you or one of your collaborators are interested in learning how to determine if a run looks good you should check out this recent post : https://blog.software.illumina.com/2021/06/14/basespace-sequence-hub-does-my-sequencing-run-look-good/. It’s dedicated to walking users through data quality analyses using the Base Space sequencing data analysis tool.
Related Posts
Avoiding a sticky situation: how cells stop messenger RNAs from clumping together
RNA Sequencing identifies new tick-borne virus that causes flu-like illness
Worm’s radical transformation shows metamorphosis can change the functions of cells
RNA sequencing reveals functional chimeric mRNAs in mammalian immunity
Atlas of the brain’s striatum could guide researchers to new drug treatments
Immune cells offer insights on billion-dollar virus
A functionally integrated cross-tissue alternative splicing program during short-term calorie restriction
Dietary oxidized plant sterol shifts macrophage state to fuel aortic inflammation
Unlocking the past – new method helps gain insights into old tissue
Novel AI model trained on RNA-Seq data accurately detects key gene mutations and predicts biomarkers across 32 cancer types
Transcriptomic aging clock reveals age-related molecular patterns in opioid dependence
RNA sequencing helps predict stem cell transplant benefit in pediatric AML
Protein ‘switch’ determines whether liposarcoma cells will become aggressive
Precursor tRNAs sense temperature changes: heat stress-induced capped pre-tRNAs suppress protein synthesis
Ketamine increases neuroplasticity in female mice but not in males
Somatic mutations linked to vascular damage in progeria
Scientists map dormant cancer cells’ hideouts, opening new targets for treatment
Soluble signals released by neighboring cells direct how the human kidney is built
Genetics influence how cancer arises – and how it evolves
RNA-based testing uncovers extraordinary diversity in mutations driving lung cancer
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