==== Class Business ==== Communicate about offloading assembler installation to Jeff and Jenny since they weren't there on Monday. Make a review articles page at a high level with citations. People can comment. Use the forum to discuss things. * Each person must sign up for the forum independently. * Forum works better than email, because you can go back later to that subject. * Email has immediate impact, but not so easily searchable. People should read the de-novo assemblers review paper so that they will be ready Friday's lecture. * (This has been added to new review articles page) * Discusses Overlap and de-Bruijn graphs. 454 Newbler assembler is entirely proprietary and almost nothing is known on how it works internally (The only description is in the supplementary material of the original 454 method paper ((Genome sequencing in microfabricated high-density picolitre reactors. Nature 2005.|http://dx.doi.org/10.1038/nature03959)). Christy Hightower wants more feedback on the tools, to say good/bad. Feedback should be added to the wiki [[lecture_notes:04-02-2010|lecture notes for her lecture]]. [[https://banana-slug.soe.ucsc.edu/feed.php|RSS feed]] for wiki. * Shows recent changes to the wiki. * See what others have been doing lately. * Good way to keep up with changes without having to scan every wiki page. ===Guest lecturers coming up:=== * Mon 19 Apr Dan Zerbino on Velvet. * Fri 23 Apr, Janet Leonard and John Pearse on Slug biology. We will talk Friday about graph representations. ==== Running on Campus Rocks ==== * Find out how much memory each tool needs. * Does it need a cluster or just a single machine? etc. Do not run anything on the headnode for campusRocks. Learn how to use sungrid to tell it how to run it on (one of) the nodes. Alternatively, use the [[http://campusrocks.soe.ucsc.edu/ganglia/|status page]] to find an idle node and ssh to it directly. The [[archive:computer_resources:campusrocks|campusrocks page]] has a link to some documentation on sungrid. We should all have access now to campusrocks. If you don't contact tech staff (IT request). For testing, there is some Pyrobaculum data on campusrocks now (or soon). * David Bernick and Kevin have been fussing with the data. * He had latest draft 4c. Have all the inversions. * Can test assemblers to see how well they work on the small genome. * 454 and Solid reads. * Go ahead and try running it. (Remember: not on the head-node.) * Start comparing the different assembly techniques. ==== Lower-level Data ==== === Instruments === * Sanger capillary * 454 * Solid * Illumina * Ion Torrent Sanger creates a trace. 454, Solid and Illumina take images with camera. Ion torrent uses direct chip pH measurement. === Traces === * 4 1-D traces (wiggles) overlapping; one for each of ACGT. * Each trace tells what there is at a position. * Peaks are broadened and end of a read is worse than beginning. * Can get several in a row that are spread out making it difficult to tell how many you have. * NCBI has large archives of trace data for abandoned projects. * Have a terminator on each seq. === Images === * The image files are enormous (TB's of data) and require a great deal of image processing. * After processing the raw images are almost never kept. * Images are typically monochrome, but SOLiD use 4 flourophores at the same time. * De-convolution problems there too. Spots may overlap. Ion Torrent has direct electronic readout, no images. === Base-calling === * For each position, turn image data into a base (AGCT) and a quality score. * Quality means something different on each platform and sometimes even each instrument (Sanger). (Correction to what I said in lecture: quality values are **supposed** to be -10 log10 P(error), but calibration is sometimes not very accurate. --- //[[karplus@soe.ucsc.edu|Kevin Karplus]] 2010/04/09 07:18//) * May have initial (known) sequences that are used to calibrate quality. === Spaces === * Base-space (A/C/G/T) * Color-space (One of four colors corresponding to the change from previous base) * Used by SOLiD * Flow-space (A/C/G/T and length of repeat) == Base-space == * Often in fasta file. * Used by Illumina. == Flow-space == * Used by sequencing-by-synthesis methods (454, Ion torrent) * Multiple of the same homo-nucleotide are added in a single step and you get a (imperfect) signal of how many. * Signal gets worse (less specific) for higher values. * Analogous to run length encoding * Often not integer values. * Ion Torrent is more linear than 454, but still has issues. * Alignments in flow-space are possible. == Color-space == * 4 colors, numbered 0 to 3. ^ number ^ binary ^ color ^ meaning ^ transitions ^ | 0 | 00 | blue | same base | (A->A C->C G->G T->T) | | 1 | 01 | green | non-complement transversion | (A->C C->A G->T T->G) | | 2 | 10 | yellow | transition | (A->G C->T G->A T->C) | | 3 | 11 | red | complement | (A->T C->G G->C T->A) | * See /cse/faculty/karplus/pluck/scripts/map-colorspace * One major reason they used this was to avoid a patent. * Allows more independence in the sequencing errors. * Binary representations are useful. * XOR is associative and commutative. * This XOR operation is also works brilliantly with the Klein four group for the bases A C G T. * You get from one base to a color, or vice versa with XOR. * A 0 00 * C 1 01 * G 2 10 * T 3 11 The di-nucleotide is simply saying, if I am at base B1 and XOR with the color C, I will get base B2, the other end of my di-nucleotide. One can define the entire SOLID color-space dinucleotide array by simply asking what color lets me XOR with my first nucleotide to get my second? Remember, it's really a series like this: ATCG is measured as chain of dinucleotide colors A -- T color3 == color 11 T -- C color2 == color 10 C -- G color3 == color 11 Each nucleotide in the final sequence is used as the right half of one dinucleotide, and then the left half of the next dinucleotide. The first letter A is given (from the last base of the first primer if it is a read). So the data actually appears something like this: (A) 3 2 3 or (00) 11 10 11 If you are on base G (10) and your next color is red (11), then your next base is simply the XOR operation, so 10 XOR 11 = 01 = C. As you move along a read or a string in color-space, you can simply keep xor-ing with the next color to get the next base! Indel in colorspace. A C G A C A A drop out GAC 1 3 2 1 1 0 A C A A (GAC deleted, 4 colors become 1 new color) 1 1 0 so 3 2 1 1 will become 3 xor 2 xor 1 xor 1 = 11 xor 10 xor 01 xor 01 = 01 == 1 which is the same as C-->A which is correct. Take the region that's changing, and the exclusive-or of it all together. Can do a lot of work directly in color-space. SNP changes colors, two changes together. A G C G (C --> T) 2 3 3 1 1 A G C A (C --> T) 2 3 1 1 3 XOR of that region has to take this base to that base. An indel maintains the two things across there, the regions are different lengths. Can do more complicated stuff, 5 long thing replaced by 3 long thing. Note that when an error happens, all bases in the read down-stream will be wrong in base-space. This is the reason that people bother to try to use color-space, because then the error stays localized. When doing SNP calling, want to know if it is a SNP or a read-error. The read-errors are independent typically.But the SNP will have coordinated changes. Either a larger change, mismapping, error, or something else. SOLID makes a big deal out of this. Not however useful for other non-SNP-calling things. Even with millions of reads, you can get false-positive SNPs at a low error rate. === Quality === Base-space, flow-space, and color-space all come with quality scores. SFF format is the flowspace format for input into the Newbler assembler. It has quality scores for each base using standard -10 log10 probability. ([[http://www.ncbi.nlm.nih.gov/Traces/trace.cgi?cmd=show&f=formats&m=doc&s=format#sff|SFF format]]) A large number of the assemblers throw away the quality data or only use it later. Some use it to just throw away reads with low quality. == Reasons for quality dropoff == * Sanger fails because of electrophoresis, not the sanger chemistry itself, as far as getting long reads. Out to about 1000 bases. * 454 synthesis starts to get out of phase. * Solid loses yield on ligation. Missing ligations. * Illumina problem with frequent washing removes template. Kevin thinks. === Memory === How do you represent this stuff in memory? Two bits per base (four possible values). With color-space, can choose them to fit what they should be. If read is not too-variable length, can fit 32 bases into a 64-bit integer. SOLID produces cs-fasta file. (cs = colorspace) It is a T (the last base of the first adapter?) T 00100 ... Sometimes we want to do matching directly in colorspace. Therefore kevin throws away the first base, and the first digit "0" above. Then he has 24-color read instead of 25-base read. But now he can match entirely in color-space. So this helps avoid problems that would otherwise happen. Sometimes don't know what strand you are working on. To get reverse-complement equivalent in color-space all you have to do is the reversal. No complementing is needed. One thing you can do when mapping is handle both strands. But you still have to hash the reversed colorspace too, so don't save memory in searches. Hashing a genome takes a lot of space. ==== Final Business ==== Journal club papers should be fairly short. Give a 10-minute summary. Will Nader want all 3 lectures next week? Or include some time for Journal Club. Start being ready to do papers middle of next week.