Biogang
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Introduction
The BioGang is an informal, distributed collection of geeky life scientists who have come together to try and think of cool problems and ideas that can be solved collaboratively. While many of us are informaticians and modelers, the Gang welcomes all comers. We have a variety of backgrounds and experiences but all share a love of science, openness and belief in the power of the web to enable distributed collaboration and community. Neil Saunders summed our approach and attitude up very well.
"A biogang characteristic: lack of respect for institutional boundaries and restrictions?"
The BioGang was created following a blog post, partially inspired by the ideafactory blog (Via a thread on the six hour startup google group
Unless otherwise stated content of the BioGang is shared under an CC-BY license and projects are likely to be open source and shared on an appropriate code repository (e.g. Google Code or GitHub)
News: Many members of The BioGang were involved in the new book Beautiful Data: The story behind elegant data solutions
Concepts
Some of the core concepts driving The BioGang are discussed below.
What is "Bursty Work"?
In the context of this Wiki, the "Burst Work" concept was inspired by a tweet by Chris Messina. He said
It just dawned on me that startups are obsolete. Sustainable, distributed bursty work is the future.
The idea is that a group of smart people can come together to start projects. These people can be spread out around the corners of the globe, working to get a project to a stage when it could be passed on to someone else or carried forward if that's the best way forward. That philosophy is sorely missing from the world of computational life science, and the hope is that this wiki will serve as a catalyst for such projects
What is an "Idea Factory"?
The concept of an idea factory in the context of bursty work is to build a collective of people and harness their collective intelligence. The days of think tanks like those at Bell Labs or PARC are long gone, but the internet allows us to bring together loosely coupled groups of people.
Pages
Members
- list of Members
External Links
- The Biogang on LinkedIn: http://www.linkedin.com/groups?gid=1300137
Recent Changes
Recent updates to the lab wiki
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31 May 2023
N 14:39 | UA Biophysics:Protocols:Carotenoid Extration ESP diffhist +423 Elizabeth Suesca talk contribs (Created page with "==Materiales para 6 gramos de célula== * Preparar centrífuga a 4 grados * 200 ml Metanol. Opcional: Agregar 2,6-Di-tert-butyl-4-methylphenol 0.1 % w/V (250 mg/250 ml) Para la extracción de carotenos, ya que los protegen de oxidación * 500 NaCl 1,7 M (99.348 g/1 L) * 200 Acetato de etilo (Mejor si esta destilado ya que tiende a ser muy hidrófilo) * Opcional Na2SO4 anhidro (1 g/ 500 ml de solución) * Cloroformo") |
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14:34 | UA Biophysics:Protocols:Carotenoid Extration 2 changes history +86 [Elizabeth Suesca (2×)] | |||
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14:24 | UA Biophysics:Protocols:K2HPO4 KH2PO4 Buffer diffhist +54 Elizabeth Suesca talk contribs |
14:23 | UA Biophysics:Protocols diffhist −7 Elizabeth Suesca talk contribs (→BUFFERS) |
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N 14:22 | UA Biophysics:Protocols:Elution Buffer 2 changes history +1,055 [Elizabeth Suesca (2×)] | |||
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14:07 (cur | prev) +588 Elizabeth Suesca talk contribs (Created page with " '''Buffer HEPES: 2 L a 400 mOsM pH 7.4 ==Materiales== MW (g/mol) [] mM mOsM M HEPES 238.30 20 20 9.532 g NaCl 58.44 170 340 19.869 g NaOH (1 M) 8 8 16 ml NaCl 16 32 1.870 g Colocar 1.6 litros de agua deionizada en la botella Pesar el HEPES y el NaCl, diluir en los 1,6 L de dH2O Ajustar pH usando NaOH a 7.4. Calcular la osmolaridad y completar los 400 mOsm con NaCl Completar los dos litros UA Biop...") |
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N 14:03 | UA Biophysics:Protocols:Calcein ESP 3 changes history +1,249 [Elizabeth Suesca (3×)] | |||
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14:03 (cur | prev) +43 Elizabeth Suesca talk contribs (→Procedimiento:) | ||||
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14:00 (cur | prev) +1,143 Elizabeth Suesca talk contribs (Created page with "'''Calceina: 400 mOsM, 50 mM, 100 ml, pH 7.4 ''' ==Materiales: == * Probeta 100 ml * 30 ml de NaOH (1M) * HCl (1M) * 3,113 g de calceina * 40 ml Buffer H: ** 5 ml de EDTA 0.2 mM (Para que quede a 0.01 mM en la solución final) ** HEPES 238.3 mg (para que quede a 10 mM en la solución final). ==Procedimiento: == # En la probeta medir 20 ml de NaOH 1M y colocar agitador # Disolver en el NaOH 3,113 g de calceina # Agregar los 40 ml del Buffer H a la calceina # A...") |
12:48 | BioMicroCenter:QC diffhist −421 Stuart S. Levine talk contribs (→AGILENT BIOANALYZER 2100) |
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08:34 | UA Biophysics:Protocols:Calcein 2 changes history −751 [Elizabeth Suesca (2×)] | |||
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08:33 (cur | prev) −804 Elizabeth Suesca talk contribs (Replaced content with " Calcein_ESP<br>") Tag: Replaced |
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08:32 | UA Biophysics:Protocols:Bacteria for Lipid Extraction 4 changes history −1,049 [Elizabeth Suesca (4×)] | |||
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N 08:31 | UA Biophysics:Protocols:Bacteria for Lipid Extraction ESP diffhist +1,206 Elizabeth Suesca talk contribs (Created page with "==Materiales para 1.4 g de célula== * Plato con SA401, máximo de un mes desde la recuperación <br> * Frasco de vidrio con 10 ml de LB<br> * 2 L de LB repartidos en 13 Erlenmeyer de 500 ml<br> ==Procedimiento== '''Dia 1''' 4:00 pm ON de SA401: una colonia en el frasco con 10 ml de LB. <br> '''Dia 2''' 8:30 am Dilución de las células: 10 ul en cada Erlenmeyer<br> '''Dia 3''' 8:30 am Concentrar la muestra <br> * Prepara la centrífuga a 4°C. <br> * Refrigerar lo...") |
06:42 | UA Biophysics:Protocols:Lipid Extraction diffhist −9 Elizabeth Suesca talk contribs |
30 May 2023
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23:52 | Hexlab 2 changes history +900 [Ximiao He (2×)] | |||
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20:13 | Holcombe:EyeTrackers 3 changes history −109 [Alex O. Holcombe (3×)] | |||
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16:25 | Lee:JC diffhist +7 Wooin Lee talk contribs (→Schedule) |
14:31 | Tomlinson:LabMeeting diffhist −726 Ryan E. Tomlinson talk contribs |
06:44 | UA Biophysics:Protocols:Lipid Extraction diffhist +89 Elizabeth Suesca talk contribs |
29 May 2023
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15:53 | CHEM-ENG590E:Wiki Textbook 9 changes history −311 [Sarah L. Perry (9×)] | |||
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15:53 | Applications of 3D Printing 2 changes history −187 [Sarah L. Perry (2×)] | |||
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15:37 | Common 3D Printing Materials 10 changes history +1,516 [Sarah L. Perry (10×)] | |||
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15:25 | BioMicroCenter:HT Tech diffhist +57 Stuart S. Levine talk contribs |
15:22 | BioMicroCenter:Sequencing diffhist −1 Stuart S. Levine talk contribs (→SHORT READ SEQUENCING) |
New Members
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- [[Category:Biogang_members]]
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