Updated README.md and WHAT_IS_NEW

[rsem.git] / README.md

diff --git a/README.md b/README.md
index 902e806821e6de5ef39eba708edf9d43c82c69ee..4184f5d44caf4d94ebb8c5445f25d531517931d8 100644 (file)
--- a/README.md
+++ b/README.md
@@ -56,6 +56,11 @@ To compile EBSeq, which is included in the RSEM package, run
 To install, simply put the rsem directory in your environment's PATH
 variable.
 
 To install, simply put the rsem directory in your environment's PATH
 variable.
 

+If you prefer to put all RSEM executables to a bin directory, please
+also remember to put 'rsem_perl_utils.pm' and 'WHAT_IS_NEW' to the
+same bin directory. 'rsem_perl_utils.pm' is required for most RSEM's
+perl scripts and 'WHAT_IS_NEW' contains the RSEM version information.
+

 ### Prerequisites
 
 C++, Perl and R are required to be installed. 
 ### Prerequisites
 
 C++, Perl and R are required to be installed. 


@@ -209,7 +214,7 @@ Here are some guidance for visualizing transcript coordinate files using IGV:
 
 1) Import the transcript sequences as a genome 
 
 
 1) Import the transcript sequences as a genome 
 

-Select File -> Import Genome, then fill in ID, Name and Fasta file. Fasta file should be 'reference_name.transcripts.fa'. After that, click Save button. Suppose ID is filled as 'reference_name', a file called 'reference_name.genome' will be generated. Next time, we can use: File -> Load Genome, then select 'reference_name.genome'.
+Select File -> Import Genome, then fill in ID, Name and Fasta file. Fasta file should be 'reference_name.idx.fa'. After that, click Save button. Suppose ID is filled as 'reference_name', a file called 'reference_name.genome' will be generated. Next time, we can use: File -> Load Genome, then select 'reference_name.genome'.

 
 2) Load visualization files
 
 
 2) Load visualization files