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Techniques and protocol discussions on sample preparation, library generation, methods and ideas
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Started by Helleaks, 11-21-2012, 03:26 AM
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1,560 views
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Started by smadbro, 03-17-2012, 08:15 AM
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3 responses
2,371 views
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by marcowanger
11-20-2012, 07:25 PM
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Started by lorendarith, 11-17-2012, 06:26 PM
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3 responses
1,572 views
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by yaximik
11-20-2012, 11:24 AM
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Started by petey, 11-15-2012, 03:59 PM
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1 response
6,214 views
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by NextGenSeq
11-19-2012, 10:00 AM
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Started by Christine90, 11-18-2012, 08:42 AM
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2 responses
7,441 views
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by TonyBrooks
11-19-2012, 05:16 AM
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Started by sujageorge, 11-15-2012, 04:49 PM
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1,832 views
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by sujageorge
11-15-2012, 04:49 PM
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Started by Turnerac0987, 09-22-2011, 05:28 AM
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22 responses
10,939 views
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by njina
11-15-2012, 02:08 AM
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Started by CC_seqanswers, 11-14-2012, 03:46 PM
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1,788 views
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Started by Jean, 11-14-2012, 07:37 AM
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1,683 views
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by Jean
11-14-2012, 07:37 AM
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Started by colinveal, 11-09-2012, 04:01 AM
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0 responses
1,880 views
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by colinveal
11-09-2012, 04:01 AM
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by SEQadmin2
Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
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by SEQadmin2
Cancer survival rates have significantly increased in the last few decades in the United States, reaching a combined 70% 5-year survival rate by 2021. Behind this number, there are years of research to find new therapies, drug targets, and early detection methods. But there is one core challenge that keeps slowing down these advances, and it’s about drug resistance.
There is no single reason why many patients don’t respond to treatment as expected. Cancer is...-
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07-08-2026, 05:17 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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07-01-2026, 11:43 AM -
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Started by SEQadmin2, 07-09-2026, 10:04 AM
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by SEQadmin2
07-09-2026, 10:04 AM
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Started by SEQadmin2, 07-08-2026, 10:08 AM
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by SEQadmin2
07-08-2026, 10:08 AM
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Started by SEQadmin2, 07-07-2026, 11:05 AM
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by SEQadmin2
07-07-2026, 11:05 AM
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