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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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27 responses
74,971 views
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by suparmin
11-07-2016, 01:02 AM
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Started by gendxdoc, 07-19-2012, 03:11 PM
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2 responses
1,916 views
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by colindaven
08-14-2012, 05:19 AM
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Started by LSC, 08-13-2012, 11:46 PM
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0 responses
1,849 views
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by LSC
08-13-2012, 11:46 PM
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Started by Comosus, 02-17-2012, 05:51 AM
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6 responses
10,694 views
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by harryzs
08-13-2012, 01:25 AM
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Script error for TopHat & Bowtie 2 for paired end and splice variant detection but?
by Richard Barker
Started by Richard Barker, 08-10-2012, 04:29 AM
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8 responses
4,883 views
0 reactions
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Last Post
by kmcarr
08-12-2012, 03:56 PM
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Started by HSV-1, 07-17-2012, 06:53 PM
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1 response
2,205 views
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Started by aggp11, 09-30-2011, 09:44 AM
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7 responses
14,363 views
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by ashuchawla
08-11-2012, 05:55 PM
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Started by julio514, 08-09-2012, 03:59 PM
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2 responses
2,212 views
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by julio514
08-10-2012, 11:23 AM
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Started by papori, 08-07-2012, 12:11 AM
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2 responses
2,158 views
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by mbblack
08-09-2012, 05:03 AM
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Started by FuzzyCoder, 02-15-2012, 11:49 PM
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11 responses
4,086 views
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by areyes
08-07-2012, 06:08 AM
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Started by chrismit, 08-06-2012, 10:14 AM
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by chrismit
08-06-2012, 10:14 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 -
Recent Articles
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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
06-18-2026, 07:11 AM -
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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.
...-
Channel: Articles
06-02-2026, 10:05 AM -
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by SEQadmin2
With the launch of new single-cell sequencing platforms in 2026, the field stands at an exciting inflection point. This article surveys the most impactful advances in the field and discusses how they’re reshaping research in cancer, immunology, and beyond.
Introduction
Single-cell sequencing technologies have undergone remarkable advances over the past decade, transitioning from low-throughput experimental approaches to highly scalable platforms capable of...-
Channel: Articles
05-22-2026, 06:42 AM -
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Started by SEQadmin2, Yesterday, 11:10 AM
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0 responses
8 views
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by SEQadmin2
Yesterday, 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
44 views
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by SEQadmin2
06-17-2026, 06:09 AM
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Sequencing the Two-Toed Sloth Genome Reveals Jumping Genes Tied to Its Extreme Metabolism
by SEQadmin2
Started by SEQadmin2, 06-09-2026, 11:58 AM
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0 responses
104 views
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by SEQadmin2
06-09-2026, 11:58 AM
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