OpEx | The OpEx pipeline | Genomics library
kandi X-RAY | OpEx Summary
kandi X-RAY | OpEx Summary
OpEx runs on Linux. It requires Python 2.7.3 or later (< Python 3) with Numpy version 1.11.0 installed and Java 1.6. At least 3 Gb of memory is required, and 8 Gb is recommended. In order to make use of the optional multithreading feature, OpEx requires a multicore CPU environment.
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Top functions reviewed by kandi - BETA
- Return the class annotation for a variant
- Return the length of the nucleotide with the given index
- Checks if the given variant is in a potential split site
- Check if this variant is outside the translated region
- Create CSNAnnot object
- Transform genomic position to CSN coordinates
- Return True if the given position is in utR
- Calculates the coordinates of the given variant
- Get a dictionary mapping transcript coordinates to transcript coordinates
- Find transcript objects for a given position
- Returns the protein sequence
- Returns the coding sequence
OpEx Key Features
OpEx Examples and Code Snippets
Community Discussions
Trending Discussions on OpEx
QUESTION
For input, I have a dictionary
...ANSWER
Answered 2021-May-24 at 11:13You can use fast third-party libraries to parse json first (orjson, ujson), then feed them into pandas as dicts. An example using orjson:
QUESTION
I have a problem with Google cloud console and kubernates
i have two projects:
...ANSWER
Answered 2021-Apr-07 at 08:38kubectl commands don't work based on gcloud project config. They work based on kubeconfig set in your local environment. To set kubeconfig to point to a particular project's cluster, run gcloud container clusters get-credentials cluster-name
command after you change your gcloud project config. Read here for more info.
QUESTION
Long question: I have two CSV files, one called SF1 which has quarterly data (only 4 times a year) with a datekey column, and one called DAILY which gives data every day. This is financial data so there are ticker columns.
I need to grab the quarterly data for SF1 and write it to the DAILY csv file for all the days that are in between when we get the next quarterly data.
For example, AAPL
has quarterly data released in SF1 on 2010-01-01 and its next earnings report is going to be on 2010-03-04. I then need every row in the DAILY file with ticker AAPL
between the dates 2010-01-01 until 2010-03-04 to have the same information as that one row on that date in the SF1 file.
So far, I have made a python dictionary that goes through the SF1 file and adds the dates to a list which is the value of the ticker keys in the dictionary. I thought about potentially getting rid of the previous string and just referencing the string that is in the dictionary to go and search for the data to write to the DAILY file.
Some of the columns needed to transfer from the SF1 file to the DAILY file are:
['accoci', 'assets', 'assetsavg', 'assetsc', 'assetsnc', 'assetturnover', 'bvps', 'capex', 'cashneq', 'cashnequsd', 'cor', 'consolinc', 'currentratio', 'de', 'debt', 'debtc', 'debtnc', 'debtusd', 'deferredrev', 'depamor', 'deposits', 'divyield', 'dps', 'ebit']
Code so far:
...ANSWER
Answered 2021-Feb-27 at 12:10The solution is merge_asof
it allows to merge date columns to the closer immediately after or before in the second dataframe.
As is it not explicit, I will assume here that daily.date
and sf1.datekey
are both true date columns, meaning that their dtype is datetime64[ns]
. merge_asof
cannot use string columns with an object
dtype.
I will also assume that you do not want the ev evebit evebitda marketcap pb pe and ps columns from the sf1
dataframes because their names conflict with columns from daily
(more on that later):
Code could be:
QUESTION
I'm trying to merge to pandas dataframes, one is called DAILY and the other SF1.
DAILY csv:
...ANSWER
Answered 2021-Feb-27 at 16:26You are facing this problem because your date
column in 'daily' and calendardate
column in 'sf1' are of type object
i.e string
Just change their type to datatime
by pd.to_datetime()
method
so just add these 2 lines of code in your Datasorting/cleaning code:-
QUESTION
I'm trying to merge two Pandas dataframes, one called SF1 with quarterly data, and one called DAILY with daily data.
Daily dataframe:
...ANSWER
Answered 2021-Feb-27 at 19:10The sorting by ticker
is not necessary as this is used for the exact join. Moreover, having it as first column in your sort_values
calls prevents the correct sorting on the columns for the backward-search, namely date
and calendardate
.
Try:
QUESTION
I have a dictionary that contains all of the information for company ticker : sector. For example 'AAPL':'Technology'.
I have a CSV file that looks like this:
...ANSWER
Answered 2021-Feb-07 at 07:29- Use
.map
, not.apply
to select values from adict
, by using a column value as akey
, because.map
is the method specifically implemented for this operation..map
will returnNaN
if the ticker is not in thedict
.
.apply
can be used, but.map
should be useddf['sector'] = df.ticker.apply(lambda x: company_dict.get(x))
.get
will returnNone
if the ticker isn't in thedict
.
QUESTION
Quick question: I am trying to do some analysis on the tickers in a CSV file.
Example of CSV file (Note that these are only the first two lines and there are around 200 tickers in total):
...ANSWER
Answered 2021-Jan-17 at 05:10QUESTION
I need to drop the majority of the companies in a historical stock market data CSV. The only companies I want to keep are 'GOOG', 'AAPL', 'AMZN', 'NFLX'. Note that there are over 20 000 companies listed in the CSV. I also want to filter out these companies while only using certain columns in the CSV. The columns are: 'ticker', 'datekey', 'assets', 'eps', 'pe', 'price', 'revenue'.
The code to filter out these companies is:
...ANSWER
Answered 2020-Dec-18 at 18:50list = ['GOOG', 'AAPL', 'AMZN', 'NFLX']
first = True
for tickers in list:
df1 = df[df.ticker == tickers]
if first:
df1.to_csv("20CompanyAnalysisData1.csv", mode='a', header=True)
first = False
else:
df1.to_csv("20CompanyAnalysisData1.csv", mode='a', header=False)
continue
QUESTION
I'm trying to copy some files from one diretory to another, check if exists and replace name if yes. And copy all files.
But it gives me the above message:
...ANSWER
Answered 2020-Nov-02 at 19:52The syntax is Copy-Item -Path "yourpathhere" -Destination "yourdestinationhere"
You've not specified path.
QUESTION
I need to remove the last element from my array. This is adulterating the results.
...ANSWER
Answered 2020-Aug-07 at 23:54As you said,
The short waythe goal is to check only if there are duplicate names.
Community Discussions, Code Snippets contain sources that include Stack Exchange Network
Vulnerabilities
No vulnerabilities reported
Install OpEx
In order to set up the pipeline correctly, we recommend running Full Installation. In Full Installation, the GRCh37 reference genome file has to be provided when running the installation script. The reference genome file will be automatically indexed by BWA and Stampy upon installation and therefore it can take a while (approx. 2-3 hours). There is also a Quick Installation option (Section 2.3). Go into the opex-v1.0.0 folder and run: ./install.py -r /path/to/reference/human_g1k_v37.fasta. where human_g1k_v37.fasta is the file of the GRCh37 reference genome sequence which (together with the corresponding .fai file) can be downloaded from the 1000G website: - ftp://ftp.1000genomes.ebi.ac.uk/vol1/ftp/technical/reference/human_g1k_v37.fasta.gz - ftp://ftp.1000genomes.ebi.ac.uk/vol1/ftp/technical/reference/human_g1k_v37.fasta.fai. Note that OpEx expects the unzipped .fasta file, and the .fai file will also need to be in the same folder as the .fasta file. Once the installation script has finished, OpEx is ready for use.
In Quick Installation one is not required to provide the reference genome, instead a path pointing to an existing genome installation can be set manually or the reference can be supplied upon the first run. Go into the opex-v1.0.0 folder and run: ./install.py. Once the installation script has finished, OpEx is ready for use. However, the GRCh37 reference genome must be set manually or supplied upon first run.
A test dataset is included with the package to confirm OpEx is installed correctly.
Input test files: Two gzipped FASTQ files (test_R1.fastq.gz, test_R2.fastq.gz) containing 372 read pairs mapping to three exons of BRCA2 and a BED file (test.bed) containing the coding exons of BRCA2 in hg19 genomic coordinates.
Expected test output files: Eleven output files generated by a correct installation of OpEx. Four files (the bash script file, the log file, the Picard metrics file, and the Platypus log file) are not included as these are dependent on the date, time, and system and are thus not informative as a test of successful installation.
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