GUI Quick Start
From PileLine
Contents |
PileLineGUI 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 position and gene 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 with SNPs.
Download the step-by-step tutorial to annotate GP files with Ensembl Genes.
