1. 3. genome analysis

2.  The first DNA-based genome to be sequenced in its entirety was that of bacteriophage Φ-X174; (5,368 bp), sequenced by Frederick Sanger in 1976
3. genome analysis

3.  The first DNA-based genome to be sequenced in its entirety was that of bacteriophage Φ-X174; (5,368 bp), sequenced by Frederick Sanger in 1976
There are several things to notice in this plot. First, the genome is circular. The density of the four nucleotides are plotted in the four outer-most circles. This density is not evenly distributed; although all four of the scales range from 0% (min., no colour) to 40% (max colour intensity), it can be easily seen that the sequence is dominated by T's (red circle), and that there are relatively few G's (outermost turquoise circle) and C's (pink circle), and a few A-rich regions (green 2nd circle). There are many genes which overlap (the genes are indicated in the "annotation circle", which is the fifth circle from the outside - with the blue bands representing genes in the forward direction).
GC Skew = (G - C)/(G + C)
AT Skew = (A - T)/(A + T)
3. genome analysis

4. exploring genome (and protein) sequences
one language
one basic tool
3. genome analysis

5. exploring genomes
3. genome analysis

6. exploring genomes
3. genome analysis

7. exploring genomes 3. genome analysis
Broad Institute of MIT and Harvard
Department of Energy Joint Genome Institute (Berkeley, USA)
Institute for Genome Sciences (University of Mariland, Baltimore USA)
3. genome analysis

8. 3. genome analysis

9. 3. genome analysis

10. In whole genome shotgun sequencing (top), the entire genome is sheared randomly into small fragments (appropriately sized for sequencing) and then reassembled. In hierarchical shotgun sequencing (bottom), the genome is first broken into larger segments. After the order of these segments is deduced, they are further sheared into fragments appropriately sized for sequencing.
3. genome analysis

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15. Circular maps of the chromosome and plasmids of enteropathogenic E
Circular maps of the chromosome and plasmids of enteropathogenic E. coli
(da Iguchi A et al. J. Bacteriol. 2009)
CDS = CoDing Sequence, region of nucleotides that corresponds to the sequence of amino acids in the predicted protein
PP = prophage: a phage (viral) genome inserted and integrated into the circular bacterial DNA chromosome
Circular maps of the chromosome and plasmids of EPEC strain E2348/69. (A) EPEC strain E2348/69 chromosome. From the outside in, the first circle shows the locations of PPs and IEs (purple, lambda-like PPs; light blue, other PPs; green, IEs and the LEE element), the second circle shows the nucleotide sequence positions (in Mbp), the third and fourth circles show CDSs transcribed clockwise and anticlockwise, respectively (gray, conserved in all eight other sequenced E. coli strains; red, conserved only in the B2 phylogroup; yellow, variable distribution; blue, E2348/69 specific), the fifth circle shows the tRNA genes (red), the sixth circle shows the rRNA operons (blue), the seventh circle shows the G+C content, and the eighth circle shows the GC skew. (B) EPEC strain E2348/69 plasmids. The boxes in the outer and inner circles represent CDSs transcribed clockwise and anticlockwise, respectively. Pseudogenes are indicated by black boxes, and other CDSs are indicated by the colors described above for panel A.
IE = integrative elements
Circular maps of the chromosome and plasmids of EPEC strain E2348/69. (A) EPEC strain E2348/69 chromosome. From the outside in, the first circle shows the locations of PPs and IEs (purple, lambda-like PPs; light blue, other PPs; green, IEs and the LEE element), the second circle shows the nucleotide sequence positions (in Mbp), the third and fourth circles show CDSs transcribed clockwise and anticlockwise, respectively (gray, conserved in all eight other sequenced E. coli strains; red, conserved only in the B2 phylogroup; yellow, variable distribution; blue, E2348/69 specific), the fifth circle shows the tRNA genes (red), the sixth circle shows the rRNA operons (blue), the seventh circle shows the G+C content, and the eighth circle shows the GC skew. (B) EPEC strain E2348/69 plasmids. The boxes in the outer and inner circles represent CDSs transcribed clockwise and anticlockwise, respectively. Pseudogenes are indicated by black boxes, and other CDSs are indicated by the colors described above for panel A.
3. genome analysis

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29. Structural genomics NMR DNA Protein Structure Algorithm
X Ray diffractometry
NMR
Residue   
THR
0.0
147.7
172.9
107.2
-125.3
187.4
CYS
123.4
63.6
103.7
PRO
60.3
83.9
-116.7
Protein Structure
cryo-electron tomography
DNA
0101# # #
#10010#1001#101
10010# #0
Algorithm
3. genome analysis