9 results in 0.0021 seconds.
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Clive Brown's Technology Talk from London Calling 2018
For the last 4 years I've attended Oxford Nanopore Technologies' yearly London Calling conference. One of the interesting bits of this conference is the... -
Priming MinION flow cell
Hi!
I've been working with the MinION from Oxford Nanopore for a small project. I used the Rapid Sequencing Kit (RAD002) and followed... -
Introducing FilterByTile: Remove Low-Quality Reads Without Adding Bias
I'd like to introduce a new member of the BBMap package, FilterByTile. It's intended to increase the quality of libraries without incurring bias, or... -
Flow cells
Wondering if anyone knows of platforms using silicon based flow cells? Only in electrical detection or also examples of fluorescence based detection using... -
Illumina MiSeq-run: Bad quality per tile. How should i interpret this fastqc-image?
I recently got very bad sequencing results from a Miseq Illumina run. The average Sequence qualities declined very early, leading to low read lengths... -
Questions Illumina technology
Hi,
Got some question regarding their technology?
1 How/ why do the prepared libraries spread equally distributed over the... -
qseq files pattern of reads with no sequence
i dont believe this is a problem, just something i'm curious about:
normally we get our data from a sequencing center that returns a fastq... -
Image re-analysis
Hi All,
We have a flow cell that we would like to re-analyze with pipeline, starting with image analysis. The reason is that this flow cell did... -
Question Re:Sequence Attachment to Illumina Flow Cell
Does anyone know how sequences are actually attached to the Illumina flow cell prior to amplification? Is it a splint ligation? The only answer I can...
