Results for "New Feature"
Bio-Scripts
...into a single file IndexFeatureFile...Creates an index for a feature file, e.g. VCF or BED fil...e reads in a file to a single new read-group. ApplyBQSR...rom a reference sequence to a new FASTA file. FindBadGenomicKm...2065 days ago
Run Pango on your multifasta file !
#More at https://cov-lineages.org/resources/pangolin/usage.html...python3.8/site-packages/sklearn/base.py:438: UserWarning: X has feature names, but DecisionTreeClassifier was fitted without feature names warnings.warn( comp...878 days ago
Install Install Gffcompare on Ubuntu / Linux
#Gffcompare is a program that is used to perform operations on general feature format (GFF) and general transfer form...813 days ago
- #R is a feature rich interpretive programming language originally released in 1995. It is heavily used in the bioinformatics community largely due to numerous R libraries a...
813 days ago
- #You typically need the corresponding genome sequence file in FASTA format. The GFF file contains information about the #features (such as genes) in the genom...
84 days ago
Python script to parse GFF file
def parse_gff(gff_file): features = [] with open(gff_file, 'r') as f:...s = line.strip().split('\t') feature = { 'seq...lit(';')) } features.append(feature) return...29 days ago
