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a frictionless surface

Thursday, February 2, 2017. What is the UCSF500? Is more than genome sequencing, but molecular profiling is an essential part of it. Recognizing this, in 2014 UC San Francisco launched the Genomic Medicine Initiative to bring high-throughput DNA and RNA sequencing techniques into routine clinical care. The first product of this effort is the UCSF500, a targeted cancer genome sequencing service that is now available to patients at the UCSF Medical Center. And other brain tumors. A rare neurological tumor.

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a frictionless surface | etalog.blogspot.com Reviews

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Thursday, February 2, 2017. What is the UCSF500? Is more than genome sequencing, but molecular profiling is an essential part of it. Recognizing this, in 2014 UC San Francisco launched the Genomic Medicine Initiative to bring high-throughput DNA and RNA sequencing techniques into routine clinical care. The first product of this effort is the UCSF500, a targeted cancer genome sequencing service that is now available to patients at the UCSF Medical Center. And other brain tumors. A rare neurological tumor.

<META> KEYWORDS

1 a frictionless surface

2 precision medicine

3 childhood gliomas

4 malignant phyllodes tumors

5 of the breast

6 peritoneal mesothelioma

7 targeted sequencing

8 the pipeline detects

9 msi detection msisensor

10 copy number alterations

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a frictionless surface,precision medicine,childhood gliomas,malignant phyllodes tumors,of the breast,peritoneal mesothelioma,targeted sequencing,the pipeline detects,msi detection msisensor,copy number alterations,fusion genes,posted by,eric t,1 comment

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a frictionless surface | etalog.blogspot.com Reviews

https://etalog.blogspot.com

Thursday, February 2, 2017. What is the UCSF500? Is more than genome sequencing, but molecular profiling is an essential part of it. Recognizing this, in 2014 UC San Francisco launched the Genomic Medicine Initiative to bring high-throughput DNA and RNA sequencing techniques into routine clinical care. The first product of this effort is the UCSF500, a targeted cancer genome sequencing service that is now available to patients at the UCSF Medical Center. And other brain tumors. A rare neurological tumor.

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etalog.blogspot.com

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etalog: Faster string concatenation in Python

http://etalog.blogspot.com/2009/07/faster-string-concatenation-in-python.html

More of a comment than a question. Monday, July 20, 2009. Faster string concatenation in Python. Pointed me to this discussion of string concatenation approaches in Python:. Efficient String Concatenation in Python. The issue here is whether adding strings together in a. Loop is inefficient enough to be worth working around. Python strings are immutable, so this:. S = 'om' for i in xrange(1000): s = 'nom'. Means doing this 1000 times:. Translate the assignment to " s = s 'nom'. Call the add method on s.

2

etalog: January 2013

http://etalog.blogspot.com/2013_01_01_archive.html

More of a comment than a question. Saturday, January 19, 2013. Overly honest methods / cheap tricks for multiple sequence alignment. What's the quickest way to get a so-so sequence alignment? Once you have this, there are plenty of efficient ways to refine the alignment, infer a tree, build a profile to search for related sequences, or any combination of these at once. MUSCLE. If some of the sequences have repetitive regions — think of paralogs from closely related species, or within a species &#82...

3

etalog: November 2014

http://etalog.blogspot.com/2014_11_01_archive.html

More of a comment than a question. Tuesday, November 4, 2014. Preview and preprint: CNVkit, copy number detection for targeted sequencing. I've posted a preprint of the CNVkit manuscript. On bioRxiv. If you think this software or method might suit your needs, please take a look and let me know what you think of it! CNVkit is a software toolkit for detecting and visualizing germline copy number variants and somatic copy number alterations in targeted or whole-exome DNA sequencing data. ( Source code.

4

etalog: October 2013

http://etalog.blogspot.com/2013_10_01_archive.html

More of a comment than a question. Tuesday, October 8, 2013. Old Cajun wisdom for the young scientist. During the summer after I started grad school, Paul Graham posted an interesting article: " Ramen Profitable. I thought it was inspiring in two ways:. The article included a vague but basically great recipe for beans and rice in the footnotes. Red and Black Beans and Rice (SEC). 8212; or —. Life of the Mind Beans and Rice (other conferences). In a rice cooker, mix together:. 1 c dry rice. Optional: 1/4 ...

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etalog: Mnemosyne: Getting Things Memorized

http://etalog.blogspot.com/2009/03/mnemosyne-getting-things-memorized.html

More of a comment than a question. Sunday, March 8, 2009. Mnemosyne: Getting Things Memorized. That brought to mind a Wired article. About Piotr Wozniak and his spaced-repetition memorization program, SuperMemo. When I originally read the article I wasn't in grad school and didn't have an urge to memorize any particular list of things. Anyway, SuperMemo appeared to be Windows-only software, and an algorithm like this would be more fun to code from scratch anyway. Enough fun, really, that there. Eric and ...

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Biopython Contributors · Biopython

http://biopython.org/wiki/Participants

Biopython version 1.67. Edit this page on GitHub. Note: People are listed here alphabetically by surname. This is only a partial listing, see also the contributor listing. In the Biopython source code or the Contributor page on GitHub. 116;iagoantao@gmail.com. Division of Biological Sciences, University of Montana. Missoula, Montana, US. Almost all programming stuff. Population genetics, Statistics, Machine learning, big data, data science. BioPopGen, testing, Python 3 zealot. Leiden, The Netherlands.

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etalog.blogspot.com

a frictionless surface

Thursday, February 2, 2017. What is the UCSF500? Is more than genome sequencing, but molecular profiling is an essential part of it. Recognizing this, in 2014 UC San Francisco launched the Genomic Medicine Initiative to bring high-throughput DNA and RNA sequencing techniques into routine clinical care. The first product of this effort is the UCSF500, a targeted cancer genome sequencing service that is now available to patients at the UCSF Medical Center. And other brain tumors. A rare neurological tumor.

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