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Techniques and protocol discussions on sample preparation, library generation, methods and ideas
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Started by Zero/1, 06-15-2018, 08:14 PM
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3 responses
2,553 views
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by Meyana
06-18-2018, 05:54 PM
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Started by SuzuBell, 06-18-2018, 01:44 PM
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1,189 views
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by SuzuBell
06-18-2018, 01:44 PM
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Started by JBKri, 10-09-2015, 07:23 AM
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5 responses
5,036 views
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by JBKri
06-14-2018, 03:46 AM
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Started by RickC7, 09-27-2017, 06:01 AM
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5 responses
2,242 views
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by RickC7
06-13-2018, 10:14 AM
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Started by Ilena Li Mura, 02-15-2013, 02:32 AM
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1 response
2,852 views
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by psreddy
06-09-2018, 12:42 AM
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Started by arctan, 12-11-2017, 09:20 AM
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12 responses
3,831 views
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by pmiguel
06-08-2018, 04:11 AM
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Started by seanw, 05-31-2018, 06:40 AM
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3 responses
1,728 views
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by ATϟGC
06-04-2018, 11:34 AM
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Started by blackknight, 05-02-2015, 02:38 AM
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1 response
2,994 views
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Started by seqtechno1, 05-30-2018, 06:06 AM
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1 response
2,823 views
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by finswimmer
05-30-2018, 08:00 PM
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Started by cement_head, 05-30-2018, 06:36 AM
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1 response
1,406 views
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Last Post
by ikripp
05-30-2018, 03:21 PM
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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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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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Yesterday, 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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07-07-2026, 11:05 AM
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