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Sequencing technologies without a commercially released platform (Oxford Nanopore, Halcyon Molecular, etc.)
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Started by lkral, 09-03-2014, 05:17 AM
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by lkral
09-03-2014, 05:17 AM
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Started by aeonsim, 02-17-2012, 02:28 AM
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51 responses
224,271 views
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by gringer
08-27-2014, 07:50 PM
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Started by BBoy, 01-16-2012, 07:44 PM
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19 responses
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by AllSeq
06-08-2014, 09:17 PM
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Started by AllSeq, 05-08-2014, 09:25 AM
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by AllSeq
05-08-2014, 09:25 AM
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Started by AllSeq, 04-21-2014, 04:16 PM
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by AllSeq
04-21-2014, 04:16 PM
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Started by GW_OK, 11-07-2012, 10:29 AM
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80 responses
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by ymc
03-21-2014, 09:38 AM
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Started by BBoy, 02-23-2014, 02:03 AM
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3 responses
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by DaleYuzuki
03-10-2014, 09:45 AM
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Started by ssully, 10-09-2012, 08:35 AM
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2 responses
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by krobison
09-13-2013, 05:06 AM
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Started by bios90, 08-24-2013, 08:51 AM
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5 responses
14,538 views
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by BBoy
09-12-2013, 09:45 PM
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Started by wanguan2000, 11-17-2010, 02:03 AM
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1 response
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by vishnuamaram
07-31-2013, 10:51 PM
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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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07-09-2026, 11:10 AM -
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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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Channel: Articles
07-01-2026, 11:43 AM -
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Started by SEQadmin2, Today, 10:26 AM
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by SEQadmin2
Today, 10:26 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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