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Rating Thread / Thread Starter	Last Post	Replies	Views
Error with per tile sequence quality (by FastQC) npawarut	04-05-2022 06:56 PM by npawarut	0	947
Up-to-date expert knowledge is the key to generating impactful biological insights ecSeq Bioinformatics	02-22-2021 03:01 AM by zainsas	1	20,528
Transferring patient's genetic testing data to the cloud: 5 myths ecSeq Bioinformatics	03-03-2020 09:47 PM by LarsB	1	7,554
Automate your Twist Human Core Exome Kit Data Analysis ecSeq Bioinformatics	01-21-2020 07:32 AM by ecSeq Bioinformatics	0	4,821
Mean Read length for RNA sequenced on Oncomine comprehensive panel mehrom01	02-25-2019 11:09 AM by mehrom01	0	11,481
Who is doing clinical sequencing here? ( 1 2) nilshomer	07-23-2018 06:30 AM by jdmendez	30	32,048
Allele frequency discrepancies in Illumina data? puggie	06-20-2018 05:25 AM by puggie	0	6,832
FDA announcement on NGS IVD for cancer Joann	11-30-2017 01:44 PM by Joann	0	8,481
Somatic Variant Reporting GERALD	02-07-2017 06:47 AM by shadowkatz	2	9,770
Final Call: Epigenetics Workshop - DNA Methylation Data Analysis (15-17 Dec 2015) ecSeq Bioinformatics	09-26-2016 03:47 AM by VC87	1	9,658
Where can I find sequencing data with known genotype? QazSeDc	05-23-2016 06:41 PM by Richard Finney	1	8,560
How many missense/nonsense per coding Mb? vasvale	04-18-2016 12:30 AM by pettervikman	4	9,201
Incidental findings according to ACMG recommendation zgene	03-14-2016 06:03 PM by uhodoglugil	1	8,714
Newbeee needs help ... from the very beginning esuarp	11-23-2015 04:51 AM by mastal	4	8,955
Upcoming NGS Workshop: A Beginner's Guide to NGS Data Analysis (early march 2015) ecSeq Bioinformatics	06-29-2015 07:31 AM by ecSeq Bioinformatics	1	11,483
LDTs on MiSeqDX foobar21	06-03-2015 11:35 AM by foobar21	0	8,579
NGS result-laboratory report disclaimer A-R-T	01-10-2015 10:27 PM by A-R-T	0	9,172
CAP Clinical NGS Checklist nilshomer	09-30-2014 07:28 PM by KevinLam	1	11,764
IonTorren PGM/Proton + Cloud vs. Illumina + Bioinformatics Core NSFICorps_EL_T2	09-30-2014 07:18 PM by KevinLam	1	11,086
Comparing read depths per gene/exon between samples shimbalama	09-10-2014 07:17 AM by bt27uk	5	9,754
Alzheimer's disease-gene database list vishnuamaram	07-21-2014 12:16 PM by Joann	4	15,928
Hands-On Training in Discovering Standard and Non-standard Transcripts ecSeq Bioinformatics	07-15-2014 05:31 AM by ecSeq Bioinformatics	1	26,636
Any labs go from non-clinical to clinical? subxero	05-02-2014 09:48 AM by subxero	0	10,485
Expression of homozygously deleted genes Gatsky	03-31-2014 05:14 AM by Gatsky	0	9,266
SNPs missing in HuGE Navigator simon_seq	02-13-2014 12:47 PM by simon_seq	0	8,972
variant database cmccabe	01-31-2014 05:47 AM by Factor	2	9,322
ISAcreatorConfigurator csmatyi	12-05-2013 07:20 AM by csmatyi	0	11,745
NGS devices get US-FDA approval GenoMax	11-29-2013 02:33 PM by ymc	4	13,827
Clinical Sequencing IT ngsAnalytics	09-05-2013 07:49 AM by ngsAnalytics	0	9,317
Clinical sequencing survey Lab7 Systems	07-16-2013 10:13 AM by Lab7 Systems	0	9,149

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