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Discussion of next-gen sequencing related bioinformatics: resources, algorithms, open source efforts, etc
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Started by laura, 05-09-2011, 04:42 AM
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35 responses
107,301 views
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by laura
12-05-2013, 02:37 AM
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Started by sci_guy, 01-23-2008, 11:19 PM
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236 responses
682,698 views
1 reaction
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by ECO
12-25-2009, 06:45 PM
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Started by gmdouglas, 06-28-2012, 01:54 PM
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2 responses
1,990 views
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by gmdouglas
07-12-2012, 10:19 AM
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Started by NicolaLosito, 04-20-2012, 09:16 AM
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4 responses
3,086 views
0 reactions
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by mkbehnke
07-12-2012, 07:17 AM
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Started by wall_y, 09-28-2011, 04:28 PM
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4 responses
5,419 views
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by drdna
07-12-2012, 06:25 AM
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Started by yuhao, 07-12-2012, 06:17 AM
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0 responses
1,613 views
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by yuhao
07-12-2012, 06:17 AM
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Started by dglemay, 06-27-2012, 04:12 PM
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5 responses
2,309 views
0 reactions
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by Simon Anders
07-12-2012, 06:12 AM
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Started by yuhao, 07-12-2012, 05:53 AM
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0 responses
1,600 views
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by yuhao
07-12-2012, 05:53 AM
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Started by dsw0002, 07-09-2012, 02:34 PM
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5 responses
5,233 views
0 reactions
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Last Post
by SES
07-12-2012, 05:51 AM
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Started by lyz1030, 07-12-2012, 05:17 AM
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2 responses
1,545 views
0 reactions
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by lyz1030
07-12-2012, 05:36 AM
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Started by ymc, 07-11-2012, 07:56 AM
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3 responses
1,657 views
0 reactions
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Last Post
by sphil
07-12-2012, 05:18 AM
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Started by sphil, 07-12-2012, 05:07 AM
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0 responses
1,892 views
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by sphil
07-12-2012, 05:07 AM
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by SEQadmin2
Childhood cancers, effectively fatal 60 years ago, are now curable for up to 85% of children with access to contemporary treatments and...-
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05-08-2026, 01:42 AM -
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by GATTACATLove this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
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Channel: Articles
07-01-2026, 11:43 AM -
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by SEQadmin2
I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.
Here are nine questions we think about, in roughly the order they matter, before...-
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by SEQadmin2
Data variability is still an issue in sequencing technologies despite the advances in reproducibility and accuracy of these platforms. But the problem does not originate in the sequencing itself, but in the previous steps, before the sample reaches the sequencer.
The first step is collection, followed by preservation and sample preparation for analysis. Most scientists overlook those steps, but not being careful might just be skewing the experiment’s results.
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Channel: Articles
06-02-2026, 10:05 AM -
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Started by SEQadmin2, Yesterday, 11:08 AM
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7 views
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by SEQadmin2
Yesterday, 11:08 AM
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Started by SEQadmin2, 06-30-2026, 05:37 AM
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0 responses
11 views
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by SEQadmin2
06-30-2026, 05:37 AM
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Started by SEQadmin2, 06-26-2026, 11:10 AM
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0 responses
19 views
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by SEQadmin2
06-26-2026, 11:10 AM
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