Minor change

docs/vcfParser.rst

@@ -1,10 +1,10 @@
 vcfParser
-=========
+==========
 Parses vcf files to reformat/add INFO fields and metaData headers and/or select entries 
 belonging to a subgroup e.g. a list of genes. Input can be piped or supplied as an infile.
 
 Usage
------
+------
 ``vcfParser.pl infile.vcf > outfile.vcf``
 
 ``vcfParser.pl infile.vcf --parseVEP 1 -rf External_Db.txt -rf_ac 3 -sf genes.v1.0.txt -sf_mc 3 -sf_ac 3,4,11,15,17,20 -sof selected_genes.vcf > outfile.vcf``
@@ -15,7 +15,7 @@ vcfParser is written in Perl, so naturally you need to have Perl installed. The
 module `Set::IntervalTree`_ is required and are used to add "ranged" annotations. 
 
 VEP
-~~~
+~~~~
 Parses the output from VEP to include RefSeq transcripts. The transcript and protein 
 annotations, moste severe consequence and gene annotations are also included in the output
 . Transcript protein predictions (Sift and Polyphen) can also be included.
@@ -26,7 +26,7 @@ A list of genes and their corresponding HGNC Symbol can be used to fork the anal
 "selected" genes and "orphan" genes.
 
 GuideLines on format for database of genes
-********************************
+*******************************************
  - The database file should contain a header line starting with "#".
  - The number of headers should match the number of field elements for each entry.
  - Do not use whitespace in headers.