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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
75,150 views
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by suparmin
11-07-2016, 01:02 AM
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Is it possible to perform RNA seq for a specific genomic region without knowing what genes are present?
by effectorpete
Started by effectorpete, 11-14-2023, 02:55 PM
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0 responses
242 views
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by effectorpete
11-14-2023, 02:55 PM
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Tutorial:How to convert raw counts to TPM for TCGA data and make a heatmap across cancer types
by crazyhottommy
Started by crazyhottommy, 10-27-2023, 03:29 PM
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0 responses
901 views
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Started by cassiemin, 06-20-2018, 11:37 AM
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3 responses
2,272 views
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by sosocute
10-26-2023, 09:52 AM
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Started by BioInfoBee, 08-23-2023, 06:14 PM
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3 responses
445 views
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by BasesBreaker
08-29-2023, 12:27 PM
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Started by malonzm1, 06-29-2023, 08:06 PM
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2 responses
475 views
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by malonzm1
08-03-2023, 01:03 AM
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Started by Diannagellar, 07-04-2023, 01:08 AM
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0 responses
198 views
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by Diannagellar
07-04-2023, 01:08 AM
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Started by crazyhottommy, 06-30-2023, 08:23 AM
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0 responses
810 views
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Started by crazyhottommy, 06-23-2023, 07:13 PM
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0 responses
311 views
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Started by Macromind101, 05-24-2023, 11:43 AM
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1 response
551 views
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by GenomicSeq
05-25-2023, 06:49 AM
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Started by [email protected], 09-05-2022, 09:47 AM
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1 response
584 views
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Last Post
by Lindsey
04-13-2023, 10:29 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...-
Channel: Webinar Series
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...-
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, 07-02-2026, 11:08 AM
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0 responses
11 views
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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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0 responses
13 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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by SEQadmin2
06-26-2026, 11:10 AM
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