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Sticky: New Resources for 1000 Genomes ( 1 2) laura	08-03-2020 05:22 PM by corintio45	37	87,396
Sticky: SEQwiki dan	06-13-2019 01:44 AM by abidalu	4	60,355
Sticky: ICGC-TCGA DREAM Somatic Mutation Calling Challenge khoulahan	01-16-2016 12:34 AM by locday123	8	118,929
Sticky: Software packages for next gen sequence analysis ( 1 2 3 ... Last Page) sci_guy	12-25-2009 06:45 PM by ECO	236	618,160

mapping hundreds of RADseq fastqs to ref genome. wbsimey	Today 02:48 PM by wbsimey	2	18
Run Kallisto on Windows 10 Brigobestia	01-21-2021 10:11 AM by Toya	1	1,754
Blastp DBv5 Entrez_query Problems Izal	01-20-2021 07:18 AM by Izal	0	130
Problem with human_g1k_v37 PandoraMid	01-15-2021 03:51 AM by hermes2014	1	968
High gap penalty in BWA annguyen	01-14-2021 12:07 PM by annguyen	0	201
gap penalty in BWA Victory	01-14-2021 07:19 AM by annguyen	1	1,909
DNA Methylation Data Analysis Workshop (April 12-15, 2021 in Berlin) ecSeq Bioinformatics	01-13-2021 12:17 AM by ecSeq Bioinformatics	0	174
Online Workshop: Bioinformatics Pipeline Development with Nextflow (May 3-6, 2021) ecSeq Bioinformatics	01-13-2021 12:11 AM by ecSeq Bioinformatics	0	173
How can I extract each APAsite possibility from this table? gcR	11-30-2020 05:59 AM by gcR	1	618
Analyzing PacBio sequel data and SRA smandape1	11-29-2020 05:47 PM by GenoMax	1	369
Genotype call incorrect in freebayes output? najoshi	11-28-2020 06:04 AM by kimaline	1	1,102
Stampy software error with PairSorter megnat	11-26-2020 05:04 AM by megnat	0	303
SUBJECT: Stampy software error with PairSorter megnat	11-26-2020 02:11 AM by megnat	0	216
Is there a tool to extract and translate sequences from a genome SeqTroubles	11-16-2020 07:00 AM by SeoSpiderCat	1	1,387
NGS data analysis - help Marko Radojkovic	11-16-2020 01:26 AM by Marko Radojkovic	0	399
Quality-, adapter- and RRBS-trimming with Trim Galore! ( 1 2 3 ... Last Page) fkrueger	11-12-2020 04:58 PM by pig_raffles	138	49,487
Arriba: Fast and accurate gene fusion detection from RNA-Seq data uhrigs	11-12-2020 08:41 AM by uhrigs	4	4,289
Are Online Trainings for NGS Data Analysis as Effective as In-person Workshops? ecSeq Bioinformatics	11-10-2020 06:31 AM by ecSeq Bioinformatics	0	463
get rsID or positions from variant name/gene info floydian_slip	11-10-2020 06:04 AM by floydian_slip	0	409
Interpreation of RSEQC read_distribution.py results richardallenfriedman	11-08-2020 02:44 PM by richardallenfriedman	0	448
Help with fasta analysis drobonz	11-08-2020 09:38 AM by drobonz	0	451
pipeline to construct alt contigs from reference contigs? tylerdodgeball	11-06-2020 04:58 PM by tylerdodgeball	1	627
mummer plot unable to parse alignment file powoods	11-05-2020 12:27 AM by jdavik	1	1,571
Constrained ordination with SNP data Marius	11-03-2020 11:45 AM by Marius	0	476
PacBio software vcf and consensus fasta do not agree Mark	10-29-2020 04:58 PM by Mark	0	528
Introducing BBDuk: Adapter/Quality Trimming and Filtering ( 1 2 3 ... Last Page) Brian Bushnell	10-29-2020 03:23 AM by Lamma	335	154,968
Obtaining gene sets for GSEA jleehan	10-27-2020 10:13 PM by stallworth	1	745
New repo sharing Broad production workflows for data processing & analysis vdauwera	10-23-2020 12:07 PM by vdauwera	0	707
MEGA software Kaskere	10-18-2020 11:06 PM by Kaskere	0	681
get cDNA start and end for exons in a list of genes floydian_slip	10-18-2020 01:34 PM by floydian_slip	0	601

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