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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
107,327 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
683,035 views
1 reaction
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by ECO
12-25-2009, 06:45 PM
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Started by Kb2013, 04-29-2015, 08:50 AM
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0 responses
1,460 views
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by Kb2013
04-29-2015, 08:50 AM
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Started by AndrewO, 04-17-2015, 10:59 AM
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2 responses
2,315 views
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by AndrewO
04-29-2015, 08:04 AM
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Started by netpumber, 04-29-2015, 06:55 AM
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1 response
1,050 views
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by GenoMax
04-29-2015, 07:10 AM
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open source s/w to asssemble de novo assembly generated contigs using reference genom
by ajagannath.patro
Started by ajagannath.patro, 01-11-2015, 10:50 PM
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4 responses
2,261 views
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by EricSchon
04-29-2015, 04:16 AM
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Started by tinguzman, 09-10-2014, 06:15 PM
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2 responses
4,207 views
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by ebioman
04-29-2015, 03:45 AM
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Started by menglin, 04-27-2015, 07:24 AM
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7 responses
2,264 views
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by menglin
04-28-2015, 11:22 PM
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Started by wdemos, 08-29-2013, 05:03 AM
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11 responses
4,769 views
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by d3d1y
04-28-2015, 08:29 PM
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Started by mnievesc, 04-09-2015, 04:21 PM
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2 responses
5,823 views
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by mnievesc
04-28-2015, 06:07 PM
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Started by ashkot, 04-28-2015, 09:12 AM
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5 responses
2,693 views
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Last Post
by GenoMax
04-28-2015, 05:17 PM
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Started by seq_GA, 02-23-2010, 12:24 AM
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22 responses
26,184 views
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Last Post
by GenoMax
04-28-2015, 05:15 PM
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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...-
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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06-02-2026, 10:05 AM -
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Started by SEQadmin2, Today, 11:05 AM
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by SEQadmin2
Today, 11:05 AM
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Started by SEQadmin2, 07-02-2026, 11:08 AM
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by SEQadmin2
07-02-2026, 11:08 AM
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Started by SEQadmin2, 06-30-2026, 05:37 AM
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by SEQadmin2
06-30-2026, 05:37 AM
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