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Sticky: New Resources for 1000 Genomes ( 1 2) laura	04-15-2017 08:48 AM by lucasrocha	36	59,918
Sticky: ICGC-TCGA DREAM Somatic Mutation Calling Challenge khoulahan	01-15-2016 11:34 PM by locday123	8	89,407
Sticky: SEQwiki dan	08-09-2010 10:56 PM by scofield_gao	3	45,283
Sticky: Software packages for next gen sequence analysis ( 1 2 3 ... Last Page) sci_guy	12-25-2009 05:45 PM by ECO	236	524,103

Introducing Clumpify: Create 30% Smaller, Faster Gzipped Fastq Files ( 1 2 3 ... Last Page) Brian Bushnell	Today 05:31 AM by GenoMax	87	13,655
Reads color in IGV seqance	07-19-2018 11:08 AM by seqance	2	134
Introducing BBDuk: Adapter/Quality Trimming and Filtering ( 1 2 3 ... Last Page) Brian Bushnell	07-19-2018 06:34 AM by jsena33	304	78,413
FASTQC warnings SK-N-BE	07-19-2018 03:59 AM by GenoMax	1	162
Bowtie 2 explanation of the pair-end mode report wariobrega	07-18-2018 10:57 PM by gopal_botany	12	19,042
HISAT2: a surprising read shows up in alignment results yip	07-18-2018 04:58 PM by yip	1	153
BBMap (aligner for DNA/RNAseq) is now open-source and available for download. ( 1 2 3 ... Last Page) Brian Bushnell	07-18-2018 06:08 AM by StephCarr	639	126,801
how to get reads with "mate mapped to a different chr" gene_x	07-18-2018 04:43 AM by splaisan	12	2,144
Ilummina data transfer from sequencer cmccabe	07-17-2018 05:50 AM by GenoMax	1	317
RepeatMasker & RepeatScout ( 1 2) Zimbobo	07-17-2018 03:12 AM by bioinfo441	39	14,953
Running STAR on Windows WSL Jandropu	07-15-2018 11:37 PM by Jandropu	2	370
How should I interpret the TMHMM/TMpret outputs? tangaheck	07-14-2018 06:00 AM by tangaheck	0	345
Understanding sailfish-cir results Sealzad	07-14-2018 05:51 AM by Sealzad	0	331
SOAP Genomics Deprecated? sstream17	07-13-2018 06:47 AM by sstream17	0	222
Run Kallisto on Windows 10 Brigobestia	07-12-2018 02:17 AM by Brigobestia	0	238
How to add GFP sequence to mouse genome for mapping Kaizen	07-11-2018 01:37 PM by atpoint	1	608
What is the process after mapping ? ugurcabuk	07-11-2018 09:59 AM by ugurcabuk	0	312
python blastxml_to_tabular.py CsprsSassyHrly	07-10-2018 02:44 PM by neavemj	3	459
High percentage of STAR unmapped reads: too short sevenless	07-10-2018 06:50 AM by sevenless	0	242
Gene set enrichment analysis for Drosophila Robby	07-10-2018 05:45 AM by Robby	0	204
Understanding Read Groups for single end and paired end data imsharmanitin	07-10-2018 03:05 AM by GenoMax	1	219
Course. Analysis of single cell RNA-seq data.25 February-1 March 2019 in Berlin (Germ Physalia-courses	07-10-2018 12:16 AM by Physalia-courses	0	157
cnv annotation svural	07-09-2018 10:37 PM by lgmSeq	1	952
CNV detection and annotation tonio100680	07-09-2018 10:31 PM by lgmSeq	2	1,817
CNV annotation tool clarissaboschi	07-09-2018 10:20 PM by lgmSeq	1	737
Annotating a genome based on CNV calls. pepsimax	07-09-2018 08:36 AM by lgmSeq	3	1,197
Introducing BBMerge: A paired-end read merger ( 1 2 3 ... Last Page) Brian Bushnell	07-09-2018 02:26 AM by GenoMax	125	44,796
Introducing Tadpole: an assembler, error-corrector, and read-extender ( 1 2 3 ... Last Page) Brian Bushnell	07-07-2018 11:46 AM by kokyriakidis	94	19,616
ViralFusionSeq not finding human-virus fusion regions rahilsethi	07-06-2018 10:21 AM by rahilsethi	0	396
Are you new to NGS and don't know where to start? - Introduction to NGS ecSeq Bioinformatics	07-06-2018 12:10 AM by ecSeq Bioinformatics	1	568

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