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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
107,288 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
682,503 views
1 reaction
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by ECO
12-25-2009, 06:45 PM
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Started by Fernas, 08-09-2014, 07:23 AM
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3 responses
3,066 views
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by hdashnow
08-09-2015, 05:01 PM
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Started by morning latte, 08-08-2015, 12:43 PM
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0 responses
901 views
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Started by fefe89, 09-11-2014, 11:43 PM
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10 responses
4,622 views
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by GenoMax
08-08-2015, 08:34 AM
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Started by andreanna05, 08-07-2015, 06:42 PM
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2 responses
2,276 views
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by andreanna05
08-08-2015, 06:24 AM
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Started by ninja_help, 08-06-2015, 02:12 PM
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4 responses
1,456 views
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by ninja_help
08-07-2015, 10:43 AM
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Started by GAV65, 08-06-2015, 12:46 PM
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5 responses
1,514 views
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by DPCook
08-07-2015, 06:21 AM
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Started by Ravaf, 08-05-2015, 06:00 AM
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4 responses
2,353 views
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by jmarshall
08-07-2015, 04:19 AM
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Started by huma Asif, 01-06-2015, 07:27 AM
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1 response
1,984 views
0 reactions
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by sumsuh
08-07-2015, 01:08 AM
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Started by alusa, 08-05-2015, 09:33 PM
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1 response
5,266 views
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by alusa
08-06-2015, 09:35 PM
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Started by sahusarika, 05-24-2015, 11:30 PM
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7 responses
2,377 views
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Last Post
by antifolate
08-06-2015, 06:23 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
9 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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