安装生物信息学软件ISQuest。前面的步骤是安装正确的。但是到了红色所示的那一步，我看不懂写的是什么，应该怎样编辑？本人Linux只是很浅显，只会按照贴出来的命令行操作。。。红色所示的步骤应该怎样进行？求解答。Read Me
This file is the user manual for ISQuest_1.4.1...
1. Building ISQuest Executable
a. Download and unzip the code in a directory.
b. Change to the directory.
c. Execute command: make
2. Installation
The ISQuest tool requires some local setup of supporting tools and databases.
2a. Installation on Windows
a. ISQuest executable file generated in step 1.
b. Download and install Microsoft Visual C++ 2010 Redistributable Package (x64)
http://www.microsoft.com/en-us/download ... x?id=14632 c. Install standalone BLAST. See manual
http://www.ncbi.nlm.nih.gov/books/NBK52637/ d. Download "nt" database and setup as instructed in step(c).
e. Edit PATH environment variable to include the path to isq executable file.
2b. Installation on Linux
a. ISQuest executable file generated in step 1.
b. Install standalone BLAST. See manual
http://www.ncbi.nlm.nih.gov/books/NBK52637/ c. Download "nt" database and setup as instructed in step(c).
d. Edit PATH environment variable to include the path to isq executable file.
2b. Installation with MPI
a. mpic++ should be in PATH.
b. Run make as usual. A new executable named mpiblast will be built.
c. Path to mpiblast must be available in the config file as MPIBLAST. This it to make sure this can be invoked from SGE. d. Set MPIHOSTCOUNT can be set. Default is 4.
e. Run isq as "qsub -pe <env> 1 isq ...."
3. User Instructions
To use the software you will need:
a. Parameter file with the following fields:
GENBANKPATH=<<SOME PATH>>
BLASTPATH=<SOME PATH>\blast-2.2.29\bin\
BLASTDB=<<SOME PATH>>\blastdb\
LOOPCOUNTER=2
USEPREVBLAST=1
MPIBLAST=/scratch/abisw001/ISQuest/isquest-code/
MPIHOSTCOUNT=8
b. A set of contigs in fasta format.
c. The set of reads used to assemble the contigs in fasta format.
d. Prefix of the name of the output files.
The command to execute the file is as follows:
>isq <paramter file> <output directory> <contig file> <read file> strain_name
4. Important Points
a. The software during the first run will download a lot of GenBank files in GENBANKPATH from NCBI.
This will make this run very slow. Future runs will be faster.
b. The software will do a BLAST search during the first run. This will make the first run slow.
Future runs can use the same BLAST results. If you want to generate new BLAST search use
USEPREVBLAST=0
c. The GBFP parser that I am using right now cannot handle certain GenBank file types.
There is no support for this anymore and I have to go in and fix the bugs.
This will be done in the next release.
5. Output Files
a. Bunch of *.sam alignment files with corresponding fasta files with same name containing the reference sequence
i. You can import them into Geneious
ii. Naming Convention <strain_name>_<loopID>_transposaseHit_<level 1 ID>_<level 2 ID>.*.sam
b. IS_Contig_Map.txt provides the contig ID and the coordinates of the original transposase hits.
就是加粗加粗加红的一行。。。我不知道怎样编辑命令来完成那一行，请高手解答
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