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1 Introduo bsica a estudos genmicos : seqenciamento e
montagem: Phred/Phrap/Consed. Bancos de dados de interesse em
bioinformtica: definies e ferramentas de submisso
21/10/2002
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-Brent Ewing, LaDeana Hillier, Michael C. Wendl, and Phil Green ; Base-Calling of
Automated Sequencer Traces Using Phred. I. Accuracy Assessment Genome Res. 1998 8:
175-185. [Abstract] [Full Text]
-Brent Ewing and Phil Green ; Base-Calling of Automated Sequencer Traces Using
Phred. II. Error Probabilities Genome Res. 1998 8: 186-194. [Abstract] [Full Text]
-David Gordon, Chris Abajian, and Phil Green ; Consed: A Graphical Tool for
ACATTTCACCTTACATAAAAAATGTGTTGAAAATTGTTAGCAAGAAACACCATAGGGCAT
CATCATCTGCTTTGTGATACATAAAACATTTGTTAAAACTGTTCTTTTCTTCTGTAAGGA
CACTCAACAGATTTATCAAATAACCATTTTAAGTGTACAATACAGTATTATTAGAGACAA
CGTTGTGTAGCAGATCTTTAGAATTTATTCATCTTGCATGATGAAAATTTTATGCCCATT
AATTAGCATTTCCCCATTTTCTCCTCCTTTCAGCCTCTAAAAGCCACCACTCTAATCTCT
GATTCTCTGAGTTTGGCAATTTTAGATACCTGGTGTGAGTAGAATCATGAAGTATTTGTA
TTTCTGTGTCTAGCTTTTTTCATTTACAATATACCTTCAAGGTTCATCCAACTTGTCACA
TATTGCAAGTTTTCCTTCTTTTTAAAGACTGAATAAAATTCCATTGTATGTATTTACCAC
ATCTTCTTTATCCATTCAGCTATCGGGCATTTACGTTGTTCCCACATCGTGACTATTTTT
AATCGTGCTA
Fragmento 3
AGAATCATGAAGTATTTGTA
TTTCTGTGTCTAGCTTTTTTCATTTACAATATACCTTCAAGGTTCATCCAACTTGTCACA
TATTGCAAGTTTTCCTTCTTTTTAAAGACTGAATAAAATTCCATTGTATGTATTTACCAC
ATCTTCTTTATCCATTCAGCTATCGGGCATTTACGTTGTTCCCACATCGTGACTATTTTT
AATCGTGCTATAATGAGCACTGGAGTGCTAATAGCTCTTTGAGATCCTGATATTTTGCTC
TTTTTTTGATAAAATGGCTTCATAATAGTTATTTCCTCATATCATTATTCTAAAAATTGA
GCTGCTAAGTATAAATCTGATCACAAAGTAAACATGTAAATATTATTTTTTAATCACACA
TGAAGGATTTTTATAGTAACTTTGTGTAAAGGTGGGTATTTTCTTGTAAGTTATTGGAAT
CTATTAATTTTAAGGGAGCATTCCAAATTTTAAGAGGTAGAAAGAAACAAAATTCCAGTG
CCTATGTAGTTTATTTCATTTTAATTTAAATTATGAGATGATTGAATAGTGTTCACATTA
GAAGTATAGGAAGATAGTTTAGAGGTCAACTTCTTTGGTCTTGTATTTCTTTTTGTTAAT
GAAATTAATGT
1- Voc usar o programa CAP para montar o contig. Mas para isso, as seqncias
devem estar em formato FASTA. Abra a pgina do BCM Search Launcher
http://searchlauncher.bcm.tmc.edu/
Escolha sequence utilities e, aps colar uma das seqncias acima no campo adequado, use a opao
ReadSeq . Observe o formato resultante. O
formato FASTA, muito usado, possui um identificador na primeira linha (aps o
>)
2- Carregue o arquivo read123.txt e salve-o no drive d:. Abra a pgina do CAP:
http://bioweb.pasteur.fr/seqanal/interfaces/cap.html ou do BCM (opo Multiple Sequences Alignment
- CAP) e carregue o arquivo
read123.txt.
3- Observe o contig formado. V pgina do BCM e escolha "pairwise sequence
alignments". Faa uma alinhamento do contig com uma das seqncias, usando
o programa BLAST ((http://www.ncbi.nlm.nih.gov) ou usando o FASTA
(http://fasta.bioch.virginia.edu/fasta/fasta_list.html)
4- Pode-se tentar fazer um alinhamento mltiplo, usando o CLUSTALW, na pgina
do BCM (http://searchlauncher.bcm.tmc.edu/)
5- Utilizando o BLAST ou o FASTA, faa uma busca num banco de dados de
nucleotdios (ex. BLASTN) . Qual o DNA mais semelhante que foi encontrado
para esse contig?
6) Considere a seqncia desconhecida 18q (clique aqui para obt-la):
Uilize os programas FGENES, GENSCAN e HMMGENE para responder as seguintes perguntas:
a)Quantos exons existem nessa seqncia? b)Quais so os pontos de incio e trmino desses
exons? c)Em que fita (normal ou reversa) se localizam esses possveis exons? d)Existem
caractersticas singulares )p. ex., seqncias de poly A? Onde esto localizadas? e)Podem ser
obtidas seqncias proteicas traduzidas a partir dessa seqncia? Qual o comprimento (em
resduos de aminocidos) dessas tradues? f) (Para HMMGENE) Podem ser obtidas tradues
alternativas para essa seqncia? Caso isto seja possvel, fornea o nmero de exons e o
comprimento da regio codificadora (CDS) para cada alternativa possvel. Observe em que fita do
DNA se encontram essas tradues alternativas.