GUI Quick Start

From PileLine

Revision as of 18:11, 21 February 2011

PileLineGUI Input Files

PileLine commands and accepted input files.

PileLineGUI is capable to handle, filter and compare genomic position files (GP) including standard pileup, BED,GFF, or VCF files.

Basically, GP are tabular files where the two first columns contain sequence name (i.e. chromosome name) and position coordinate respectively. Additional optional fields are accepted in PileLineGUI, see an example of GP input file below:

chr10     118829     optional1     optional2     optional3     ...    
chr10     121207     optional1     optional2     optional3     ...
chr10     121337     optional1     optional2     optional3     ...
chr10     121636     optional1     optional2     optional3     ...

PileLineGUI Guided Example #1

1. Download and uncompress GP files (pileup format) and Annotation files to your working directory:

REFERENCE GENOME

• Human Genome 18 in FASTA (.fa) and indexed FASTA (.fai). The sequence names are without the 'chr' prefix.

hg18.zip (929MB)

EXPERIMENT FILES

• GP files-Experiment 1. Each .zip file contains 2 files: a complete and a variants-only pileup.

Control1Files.zip (36MB)

Case1Files.zip (36MB)

Note: there is only data for the chromosome 10

• GP files-Experiment 2. Each .zip file contains 2 files: a complete and a variants-only pileup.

Control2Files.zip (38MB)

Case2Files.zip (38MB)

Note: there is only data for the chromosome 10

ANNOTATION FILES

• Gene Annotation .BED file.Ensembl Genes for the Human Genome 18.

Hg18_hgnc_ensembl_genes.bed.zip (365KB)

• SNPs from dbSNP version 36.3 for the Human Genome 18.

DbSNP_36.3.bed.bgz.zip (150MB)

2. Compare 2 samples at variant level using 2smc.sh functionality.

Download the step-by-step tutorial to run 2smc functionality.

3. Compare N samples at variant level using nsmc.sh functionality.

Download the step-by-step tutorial to run nsmc functionality.

4. Annotate GP files.

Download the step-by-step tutorial to annotate GP files.