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Rating Thread / Thread Starter	Last Post	Replies	Views
Allele frequency discrepancies in Illumina data? puggie	06-20-2018 06:25 AM by puggie	0	2,418
Alzheimer's disease-gene database list vishnuamaram	07-21-2014 01:16 PM by Joann	4	11,156
Any labs go from non-clinical to clinical? subxero	05-02-2014 10:48 AM by subxero	0	6,103
CAP Clinical NGS Checklist nilshomer	09-30-2014 08:28 PM by KevinLam	1	7,150
Clinical Sequencing IT ngsAnalytics	09-05-2013 08:49 AM by ngsAnalytics	0	4,901
Clinical sequencing survey Lab7 Systems	07-16-2013 11:13 AM by Lab7 Systems	0	4,742
Comparing read depths per gene/exon between samples shimbalama	09-10-2014 08:17 AM by bt27uk	5	5,225
Expression of homozygously deleted genes Gatsky	03-31-2014 06:14 AM by Gatsky	0	4,862
FDA announcement on NGS IVD for cancer Joann	11-30-2017 02:44 PM by Joann	0	3,904
Final Call: Epigenetics Workshop - DNA Methylation Data Analysis (15-17 Dec 2015) ecSeq Bioinformatics	09-26-2016 04:47 AM by VC87	1	5,007
Hands-On Training in Discovering Standard and Non-standard Transcripts ecSeq Bioinformatics	07-15-2014 06:31 AM by ecSeq Bioinformatics	1	22,022
How many missense/nonsense per coding Mb? vasvale	04-18-2016 01:30 AM by pettervikman	4	4,637
Incidental findings according to ACMG recommendation zgene	03-14-2016 07:03 PM by uhodoglugil	1	4,310
Incidental Findings via Next Gen Sequencing in Human Subject Research Joann	11-05-2012 11:06 PM by Sequer	1	5,238
IonTorren PGM/Proton + Cloud vs. Illumina + Bioinformatics Core NSFICorps_EL_T2	09-30-2014 08:18 PM by KevinLam	1	6,653
ISAcreatorConfigurator csmatyi	12-05-2013 08:20 AM by csmatyi	0	7,416
LDTs on MiSeqDX foobar21	06-03-2015 12:35 PM by foobar21	0	4,150
Mean Read length for RNA sequenced on Oncomine comprehensive panel mehrom01	02-25-2019 12:09 PM by mehrom01	0	3,691
Newbeee needs help ... from the very beginning esuarp	11-23-2015 05:51 AM by mastal	4	4,442
NGS devices get US-FDA approval GenoMax	11-29-2013 03:33 PM by ymc	4	9,186
NGS result-laboratory report disclaimer A-R-T	01-10-2015 11:27 PM by A-R-T	0	4,545
SNPs missing in HuGE Navigator simon_seq	02-13-2014 01:47 PM by simon_seq	0	4,520
Somatic Variant Reporting GERALD	02-07-2017 07:47 AM by shadowkatz	2	5,273
The Clinical Partner Program EdgeBio	11-08-2012 01:15 PM by EdgeBio	0	5,612
Up-to-date expert knowledge is the key to generating impactful biological insights ecSeq Bioinformatics	07-31-2015 06:58 AM by ecSeq Bioinformatics	0	4,178
Upcoming NGS Workshop: A Beginner's Guide to NGS Data Analysis (early march 2015) ecSeq Bioinformatics	06-29-2015 08:31 AM by ecSeq Bioinformatics	1	6,719
variant database cmccabe	01-31-2014 06:47 AM by Factor	2	4,969
Website to find variants associated with a disease BAMseek	05-23-2013 01:34 PM by BAMseek	0	5,619
Where can I find sequencing data with known genotype? QazSeDc	05-23-2016 07:41 PM by Richard Finney	1	3,976
Who is doing clinical sequencing here? ( 1 2) nilshomer	07-23-2018 07:30 AM by jdmendez	30	20,740

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