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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
107,289 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
682,525 views
1 reaction
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by ECO
12-25-2009, 06:45 PM
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Started by RocheKermit, 11-05-2012, 08:41 AM
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1 response
2,742 views
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by yingzhang
11-27-2012, 12:24 PM
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Started by Genomics101, 11-27-2012, 08:20 AM
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2 responses
1,666 views
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by Genomics101
11-27-2012, 11:35 AM
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Started by mattarno, 11-23-2012, 08:30 AM
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5 responses
5,762 views
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by westerman
11-27-2012, 10:52 AM
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Started by Amative, 11-27-2012, 09:41 AM
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0 responses
1,316 views
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by Amative
11-27-2012, 09:41 AM
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Started by jstjohn, 11-27-2012, 09:09 AM
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0 responses
1,528 views
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by jstjohn
11-27-2012, 09:09 AM
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Started by jorhodes, 11-27-2012, 05:02 AM
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4 responses
2,362 views
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by jorhodes
11-27-2012, 07:40 AM
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Started by honey, 11-27-2012, 06:00 AM
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1 response
1,456 views
0 reactions
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by kopi-o
11-27-2012, 06:59 AM
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Started by Jetse, 11-27-2012, 06:47 AM
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0 responses
1,372 views
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Last Post
by Jetse
11-27-2012, 06:47 AM
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Started by nans_bn, 11-27-2012, 05:16 AM
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0 responses
2,706 views
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by nans_bn
11-27-2012, 05:16 AM
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Started by lflc, 11-06-2012, 04:01 AM
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3 responses
1,852 views
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Last Post
by RickBioinf
11-27-2012, 01:37 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
Yesterday, 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...-
Channel: Articles
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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, 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
18 views
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by SEQadmin2
06-26-2026, 11:10 AM
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Whole-Genome Sequencing Traces Faroe Islands Ancestry to a North Atlantic Founder Population
by SEQadmin2
Started by SEQadmin2, 06-17-2026, 06:09 AM
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0 responses
52 views
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Last Post
by SEQadmin2
06-17-2026, 06:09 AM
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