improve documentation
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18
readme.md
18
readme.md
@@ -85,6 +85,8 @@ four sequences: Alpha CDR3, Beta CDR, Alpha CDR1, Beta CDR1. The sequences are r
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random integers. CDR3 Alpha and Beta sequences are all unique. CDR1 Alpha and Beta sequences
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random integers. CDR3 Alpha and Beta sequences are all unique. CDR1 Alpha and Beta sequences
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are not necessarily unique; the relative diversity can be set when making a Cell Sample file.
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are not necessarily unique; the relative diversity can be set when making a Cell Sample file.
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(Note: though cells still have CDR1 sequences, matching of CDR1s is currently awaiting re-implementation.)
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Options when making a Cell Sample file:
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Options when making a Cell Sample file:
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* Number of T cells to generate
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* Number of T cells to generate
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* Factor by which CDR3s are more diverse than CDR1s
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* Factor by which CDR3s are more diverse than CDR1s
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@@ -95,17 +97,13 @@ Comments are preceded by `#`
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Structure:
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Structure:
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---
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---
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# Sample contains 1 unique CDR1 for every 4 unique CDR3s.
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# Sample contains 1 unique CDR1 for every 4 unique CDR3s.
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| Alpha CDR3 | Beta CDR3 | Alpha CDR1 | Beta CDR1 |
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| Alpha CDR3 | Beta CDR3 | Alpha CDR1 | Beta CDR1 |
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|---|---|---|---|
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|---|---|---|---|
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|unique number|unique number|number|number|
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|unique number|unique number|number|number|
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---
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---
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**NOTE:** Matching of CDR1s is currently awaiting re-implementation.
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#### Sample Plate Files
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#### Sample Plate Files
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Sample Plate files consist of any number of "wells" containing any number of T cells (as
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Sample Plate files consist of any number of "wells" containing any number of T cells (as
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described above). The wells are filled randomly from a Cell Sample file, according to a selected
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described above). The wells are filled randomly from a Cell Sample file, according to a selected
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@@ -163,15 +161,15 @@ the accuracy of BiGpairSEQ simulations) and a Sample Plate file (to construct th
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occupancy graph). These files can be several gigabytes in size. Writing them to a file lets us generate a graph and
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occupancy graph). These files can be several gigabytes in size. Writing them to a file lets us generate a graph and
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its metadata once, then use it for multiple different BiGpairSEQ simulations.
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its metadata once, then use it for multiple different BiGpairSEQ simulations.
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These files do not have a human-readable structure, and are not portable to other programs.
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(Export of graphs in a portable data format may be implemented in the future.
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Exporting the graph itself is easy, the tricky part is packaging it with the necessary metadata.)
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Options for creating a Graph and Data file:
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Options for creating a Graph and Data file:
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* The Cell Sample file to use
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* The Cell Sample file to use
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* The Sample Plate file (generated from the given Cell Sample file) to use.
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* The Sample Plate file (generated from the given Cell Sample file) to use.
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These files do not have a human-readable structure, and are not portable to other programs. (Export of graphs in a
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portable data format may be implemented in the future. The tricky part is encoding the necessary metadata.)
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---
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#### Matching Results Files
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#### Matching Results Files
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Matching results files consist of the results of a BiGpairSEQ matching simulation.
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Matching results files consist of the results of a BiGpairSEQ matching simulation.
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Files are in CSV format. Rows are sequence pairings with extra relevant data. Columns are pairing-specific details.
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Files are in CSV format. Rows are sequence pairings with extra relevant data. Columns are pairing-specific details.
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@@ -188,7 +186,7 @@ Options when running a BiGpairSEQ simulation of CDR3 alpha/beta matching:
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* given value from 0 to 100
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* given value from 0 to 100
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* (To skip using this filter, enter 0)
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* (To skip using this filter, enter 0)
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Sample File Structure:
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Example output:
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---
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---
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```
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```
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