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	Topics		Statistics	Last Post
	Error with per tile sequence quality (by FastQC) by npawarut Started by npawarut, 04-05-2022, 06:56 PM		0 responses 1,217 views 0 likes	Last Post by npawarut 04-05-2022, 06:56 PM
	The Next Generation Sequencing Advances Liquid Biopsy Companion Diagnostics by vivianshaw Started by vivianshaw, 12-07-2021, 08:02 PM		0 responses 2 views 0 likes	Last Post by vivianshaw 12-07-2021, 08:02 PM
	Up-to-date expert knowledge is the key to generating impactful biological insights by ecSeq Bioinformatics Started by ecSeq Bioinformatics, 07-31-2015, 05:58 AM		1 response 21,059 views 0 likes	Last Post by zainsas 02-22-2021, 04:01 AM
	Transferring patient's genetic testing data to the cloud: 5 myths by ecSeq Bioinformatics Started by ecSeq Bioinformatics, 02-29-2020, 01:41 AM		1 response 7,594 views 0 likes	Last Post by LarsB 03-03-2020, 10:47 PM
	Automate your Twist Human Core Exome Kit Data Analysis by ecSeq Bioinformatics Started by ecSeq Bioinformatics, 01-21-2020, 08:32 AM		0 responses 4,865 views 0 likes	Last Post by ecSeq Bioinformatics 01-21-2020, 08:32 AM
	Mean Read length for RNA sequenced on Oncomine comprehensive panel by mehrom01 Started by mehrom01, 02-25-2019, 12:09 PM		0 responses 11,521 views 0 likes	Last Post by mehrom01 02-25-2019, 12:09 PM
	Who is doing clinical sequencing here? by nilshomer Started by nilshomer, 08-27-2012, 02:46 PM		30 responses 32,150 views 0 likes	Last Post by jdmendez 07-23-2018, 06:30 AM
	Allele frequency discrepancies in Illumina data? by puggie Started by puggie, 06-20-2018, 05:25 AM		0 responses 6,870 views 0 likes	Last Post by puggie 06-20-2018, 05:25 AM
	FDA announcement on NGS IVD for cancer by Joann Started by Joann, 11-30-2017, 02:44 PM		0 responses 8,518 views 0 likes	Last Post by Joann 11-30-2017, 02:44 PM
	Somatic Variant Reporting by GERALD Started by GERALD, 09-07-2016, 10:45 AM		2 responses 9,812 views 0 likes	Last Post by shadowkatz 02-07-2017, 07:47 AM

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