User: abdul.suboor123
abdul.suboor123 • 0
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Posts by abdul.suboor123
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... @Bastien Hervé , I have a little knowledge of Python, but I am not good at python. Yes I have SnapGene sequences and sanger sequeced files. Please tell me the trick how I can do that? Yeah for each sequence I need a junction in sanger sequence. ...
written 4 weeks ago by
abdul.suboor123 • 0
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... For Example the SnapGene Sequence is:
CTTGAAGTTATTGATAACATACTCTTAAAAATGACTGAGGAAGAATCTGCTGTGGCCGCTGCTAGCACAGGCACTGAAAAGGGGAAAAAACAAGCTGAAGACATTTTGGAGGGTGAAGATTTCGAATTTCAAGATCTACTTGGGCAAGAGCTGACAGACGCTGAAAAAGCAGAGCTTAAAAGATGTGCCATAGCCTGCGGATATAAGCCAGGGGCTACACTATTTGGTGGGGTTAACGAAGGAAAGCTGAG ...
written 5 weeks ago by
abdul.suboor123 • 0
• updated
5 weeks ago by
Bastien Hervé ♦ 3.3k
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... Yes you are right, if AAAAACGCGCGCGCCCCC is circDNA sequence, with snapgene when select the circular option, it create a junction site, means it connect the start and end of the circDNA sequence, i.e. junction site from the sequence is CCCCCAAAAA. These ten basis I want to confirm from the sanger se ...
written 5 weeks ago by
abdul.suboor123 • 0
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... I have tried blast and it shows that the sequence more than 90% belong to maize genome, but I want to validate its cicularity, whether it is circled or not??I know that the sequence is right, but acutally need to confirm the circularity of the DNA sequence which resulted after the application of the ...
written 5 weeks ago by
abdul.suboor123 • 0
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... For example: I have sequenced my circDNA samples of maize crop, I have analysed the data with two softwares CIRI and CIRCexplorer2 and it resulted that I have 150 circDNAs from CIRI and 188 from CIRCexplorer results. Now I want to confirm that if the sequence of circDNA is really a maize line sequen ...
written 5 weeks ago by
abdul.suboor123 • 0
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... My objective is to validate my circDNA data, If there is any other way please tell me. Can you tell me about the script use for validation through python or perl? ...
written 5 weeks ago by
abdul.suboor123 • 0
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... My NGS data is in fastQ format, whereas the sanger sequence data is in EditSeq file format. I have selected some junction reads through bedtools and then make primers for each read, and make sanger sequencing, this procedure I learn from my labmate, she perform it on circRNA data. my data is circDNA ...
written 5 weeks ago by
abdul.suboor123 • 0
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... I have done analysis of circDNA NGS data, now I am validating the circDNA sequence reads with sanger sequence, but this is my 5th time I am trying on notepad++, in "find" option I put the junction site "five bases from start and five bases from end" of my circDNA sequence read, but it doesn't match. ...
written 5 weeks ago by
abdul.suboor123 • 0
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... @Kevin Blighe Thank you, I will try on those packages mentioned in the nature article. ...
written 12 weeks ago by
abdul.suboor123 • 0
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... Thanks @Kevin Blighe , I visited the link you provided, but there is no any solution about the problem, they are also still trying to develop it. Yeah At least I came to know that they are still developing it , not yet developed. Thanks. ...
written 12 weeks ago by
abdul.suboor123 • 0
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