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Sticky: SEQwiki dan	06-13-2019 01:44 AM by abidalu	4	55,512
Sticky: New Resources for 1000 Genomes ( 1 2) laura	04-15-2017 09:48 AM by lucasrocha	36	77,904
Sticky: ICGC-TCGA DREAM Somatic Mutation Calling Challenge khoulahan	01-16-2016 12:34 AM by locday123	8	109,188
Sticky: Software packages for next gen sequence analysis ( 1 2 3 ... Last Page) sci_guy	12-25-2009 06:45 PM by ECO	236	587,033

GATK: Calling variants on chromosome Y dfermin315	02-25-2020 07:42 AM by m_two	1	240
4th Berlin Summer School in NGS Data Analysis, June 15-19, 2020 ecSeq Bioinformatics	02-23-2020 11:28 PM by ecSeq Bioinformatics	0	166
bbmap.sh: line 352 RANDOM# Killed jylee	02-22-2020 04:26 AM by GenoMax	1	346
featureCounts: a universal read summarization program ( 1 2 3 ... Last Page) shi	02-20-2020 04:21 PM by mazoilya	155	62,632
Noob question: semantics between terms dent	02-19-2020 11:51 PM by GSviral	3	456
Tassel 5 installation error benitro	02-19-2020 12:20 AM by ubs717	10	1,416
How to properly concatenate reads from PE sequencing files for alignment AngryDutchman	02-18-2020 08:55 AM by AngryDutchman	0	168
GATK Germline CNV caller zgene	02-15-2020 06:27 AM by zgene	0	275
How many reads/replicates do I need for bacterial RNA-seq? MiSeq? turnersd	02-14-2020 01:29 PM by dmking	4	9,317
find variants compared to sequenced reference lorenzo.C	02-14-2020 04:38 AM by GenoMax	3	610
concatenating fasta files with TAB seperating loci schwentner	02-13-2020 09:45 AM by kmcarr	2	435
RNA-Seq Time series analysis in EdgeR josmantorres	02-13-2020 05:21 AM by josmantorres	0	265
featureCounts output format error slefevre	02-12-2020 04:14 AM by slefevre	0	183
How to select batch correction features for single cell RNA seq? getanid123	02-11-2020 08:16 PM by getanid123	0	193
Confusing Picard HsMetrics ON_BAIT_VS_SELECTED for near=250 and near=0 floydian_slip	02-11-2020 01:12 PM by floydian_slip	0	213
Convert vcf to bed based on PS field bhumika	02-10-2020 05:13 AM by bhumika	0	400
Pfam search using hmmer but only for a specific taxonomy polaxgr	02-10-2020 03:19 AM by polaxgr	0	375
SPAdes assembler bioramg	02-09-2020 08:28 PM by SNPsaurus	1	316
DEXSeq errors with the sample data bbm	02-09-2020 05:53 PM by bbm	0	213
What is the cuffdiff output really telling you? turnersd	02-08-2020 09:30 AM by bbm	8	12,127
Pipelines for low coverage genomes oiiio	02-07-2020 10:32 AM by oiiio	0	451
bioinformatic assignment help -Rheumatoid arthritis undergradmolly	02-06-2020 06:41 AM by undergradmolly	0	218
Human read filtering with Kraken 2 JasperGeh	02-06-2020 12:36 AM by JasperGeh	2	281
Read deduplication with extremely high coverage and variant calling Mike2188	02-04-2020 08:00 AM by Mike2188	2	390
16S rRNA emlas	02-03-2020 05:23 PM by GenoMax	4	410
FastQ aligner emlas	02-03-2020 06:18 AM by GenoMax	1	265
Need help with MHC-1 & 2 HLA binding prediction for multiple sequences and alleles. screadore	02-02-2020 06:55 PM by yisoo	3	1,108
SOAPdenovo2 long run Phoenix	01-31-2020 11:01 PM by Phoenix	2	624
length of uniquely mapped seq in Bismark Hedi86	01-31-2020 05:26 AM by Hedi86	4	475
How to get variant allele frequency for internal tandem duplications from Pindel? myourshaw	01-30-2020 09:29 AM by myourshaw	0	276

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