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Maybe your problem is related to an outdated XML::SAX? (first note). Just an idea.. -
Yea, I know but I don't do the blast updates for our system and so can't take that route to a fix. Thanks for trying to help though.Leave a comment:
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Subject description. Yes I know you could grab the oridinal ID and the go back to the blastdb and pull out the record and parse it's description from there but that's a bit of a pain so I would rather find out if there is a solution to the parsing of the xml output.Leave a comment:
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What do you mean by hit description? There are like 40 fields to choose from..Originally posted by Mark View PostLast edited by rhinoceros; 04-27-2013, 10:16 AM.Leave a comment:
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Unfortunately, you can't get the hit description via that method, a serious shortcoming.Leave a comment:
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Can't really help you there but have you considered other output formats (e.g. outfmt 6) and simply parsing your files with unix commands?Leave a comment:
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bioperl blast parsing problem
We recently upgraded our installation of blast from v2.2.19 to blast+ 2.2.26 and I have found that my bioperl blast xml parsers no longer work properly (typically they return some form of truncated result). Has anyone else encountered this and if this is a known problem have either the NCBI or BioPerl folks provided a solution.
Thanks
Mark
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Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
...07-09-2026, 11:10 AM -
Cancer survival rates have significantly increased in the last few decades in the United States, reaching a combined 70% 5-year survival rate by 2021. Behind this number, there are years of research to find new therapies, drug targets, and early detection methods. But there is one core challenge that keeps slowing down these advances, and it’s about drug resistance.
There is no single reason why many patients don’t respond to treatment as expected. Cancer is...07-08-2026, 05:17 AM -
Love this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.07-01-2026, 11:43 AM
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