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Application of sequencing to RNA analysis (RNA-Seq, whole transcriptome, SAGE, expression analysis, novel organism mining, splice variants)
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Started by jgoecks, 11-29-2010, 02:06 PM
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by suparmin
11-07-2016, 01:02 AM
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Started by maryam, 12-26-2015, 08:44 AM
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by maryam
12-26-2015, 08:44 AM
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Started by smm, 12-23-2015, 12:49 AM
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by smm
12-23-2015, 12:49 AM
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Started by abaldor, 12-21-2015, 02:14 PM
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1 response
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by abaldor
12-21-2015, 02:26 PM
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Started by jhsandgren, 04-26-2013, 05:19 AM
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5 responses
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by avi.sri
12-19-2015, 02:00 PM
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Started by Studentlost, 12-16-2015, 01:59 PM
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by dpryan
12-17-2015, 12:36 AM
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Started by lre1234, 12-15-2015, 08:24 AM
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1 response
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by alexdobin
12-16-2015, 01:31 PM
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Started by erickson, 06-19-2014, 08:30 AM
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1 response
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by jsage8
12-16-2015, 12:41 PM
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Started by Pinal, 12-10-2015, 11:38 PM
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4 responses
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by Pinal
12-11-2015, 02:22 AM
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Various analysis we can do after the Denovo assembly of Transcriptome sequencing data
by sequencer.boy
Started by sequencer.boy, 12-10-2015, 10:39 PM
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1 response
1,881 views
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by GenoMax
12-11-2015, 01:47 AM
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Started by jjovel, 12-10-2015, 12:24 PM
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by SylvainL
12-11-2015, 01:43 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, 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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Started by SEQadmin2, 06-26-2026, 11:10 AM
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by SEQadmin2
06-26-2026, 11:10 AM
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