Version Differences for S. pneumoniae

Line 1:
    + =S. pneumoniae=  
    + Streptococcus pneumoniae TIGR4. The S. pneumoniae TIGR4 consists of a circular chromosome of 2,160,842 bp in length.  
       
    + ==Website data==  
    + The Illumina and pacbio data were downloaded from ALLPATHS-LG website : [ftp://ftp.broadinstitute.org/pub/papers/assembly/Ribeiro2012/data/strep_data.tar.gz strep_data.tar.gz] <br>  
       
    + ===Fragment library===  
    + Reads length : 101bp <br>  
    + Reads amount : 1067060 X2 <br>  
    + Insert size : 180bp <br>  
    + Coverage : 88.89X  
    + ===Jumping library===  
    + Reads length : 93bp <br>  
    + Reads amount : 1161883 X2 <br>  
    + Insert size : 3000bp <br>  
    + ===PacBio reads===  
    + Reads average length : 1159.12bp <br>  
    + Reads amount : 403745 <br>  
    + Coverage : 216.58X <br>  
    + ==Raw data==  
    + The raw data of website data from Sequence Read Archive (SRA)  
       
    + ===Fragment library===  
    + Accession : [http://www.ncbi.nlm.nih.gov/sra/SRX110128 SRX110128] <br>  
    + Reads length : 101bp <br>  
    + Reads amount : 5706200 X2 <br>  
    + Insert size : 180bp <br>  
    + Coverage : 475.33X <br>  
    + ===Jumping library===  
    + Accession : [http://www.ncbi.nlm.nih.gov/sra/SRX105406 SRX105406] <br>  
    + ===PacBio reads===  
    + Accession : [http://www.ncbi.nlm.nih.gov/sra/SRX109959 SRX109959],[http://www.ncbi.nlm.nih.gov/sra/SRX109958 SRX109958]  
    + ==Self-fraction data==  
    + We randomly selected the same fraction as website data from fragment and jumping library of raw data by prepare.sh.  
       
    + PrepareAllPathsInputs.pl\  
    + DATA_DIR=$PWD/test.genome/data\  
    + PLOIDY=1\  
    + FRAG_FRAC=0.187\  
    + JUMP_FRAC=0.558\  
    + IN_GROUPS_CSV=in_groups.csv\  
    + IN_LIBS_CSV=in_libs.csv\  
    + OVERWRITE=True\  
    + | tee prepare.out  
    + ==100X fragment reads==  
    + We randomly selected 100X coverage data from fragment library of raw data by prepare.sh.  
       
    + Fragment library fraction = 100/475.12 = 0.21 <br>  
       
    + PrepareAllPathsInputs.pl\  
    + DATA_DIR=$PWD/test.genome/data\  
    + PLOIDY=1\  
    + FRAG_FRAC=0.21\  
    + JUMP_FRAC=0.558\  
    + IN_GROUPS_CSV=in_groups.csv\  
    + IN_LIBS_CSV=in_libs.csv\  
    + OVERWRITE=True\  
    + | tee prepare.out  
       
    + We also use another setting with all jumping library reads.  
       
    + PrepareAllPathsInputs.pl\  
    + DATA_DIR=$PWD/test.genome/data\  
    + PLOIDY=1\  
    + FRAG_FRAC=0.21\  
    + IN_GROUPS_CSV=in_groups.csv\  
    + IN_LIBS_CSV=in_libs.csv\  
    + OVERWRITE=True\  
    + | tee prepare.out