Molecular Fingerprinting encodes a Simplified Molecular Input Line Entry Specification (SMILES) as a fingerprint. The fingerprint can represent elements, atom pairs, or functional groups, etc., and are often used for substructure searches and similarity searches in drug discovery.
This operator uses [RDKit](https://www.rdkit.org/docs/index.html) to generate the molecular fingerprint.
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## Code Example
An example that use the Morgan algorithm to generate a fingerprint of the molecular formula 'Cc1ccc(cc1)S(=O)(=O)N'.
*Write a same pipeline with explicit inputs/outputs name specifications:*
Create the operator via the following factory method:
***molecular_fingerprinting.rdkit( algorithm: str = 'morgan', size: int = 2048)***
**Parameters:**
***algorithm:*** *str*
Which algorithm to use for fingerprinting, including 'morgan', 'daylight', 'ap', 'maccs', defaluts to 'morgan', and there is the [list of available fingerprints](https://www.rdkit.org/docs/GettingStartedInPython.html#list-of-available-fingerprints).
***size:*** *int*
The bit vector size just for morgan and daylight algorithm, defaults to 2048.
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## Interface
An molecular fingerprinting operator takes a SMILES as input.
It uses the RDKit specified by algorithm name to generate a SMILES fingerprint.
**Parameters:**
***smiles:*** *str*
A Simplified Molecular Input Line Entry Specification (SMILES).
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