Are you interested in getting started in #bioinformatics but not sure where to begin? Here are some tips to help you get started on your journey. A THREAD🧵🧵:
Next, learn about #genomic data formats and standards, such as #FASTA, #FASTQ, and #GFF. This will allow you to effectively manipulate and analyze large-scale #genomic#datasets. The #NCBI SRA and #EBI ENA databases are great places to find real-world data to work with.
Keep up to date with the latest research in the field by reading papers and attending conferences and workshops, such as the #ISMB conference series.
Consider pursuing advanced training or certification in #bioinformatics, such as a graduate degree or specialized coursework. Programs like the one at Johns Hopkins University are highly regarded in the field.
Developing a strong understanding of the ethical and privacy considerations surrounding #genomic#data is crucial. Make sure to read up on best practices and guidelines, such as those outlined by the National Human Genome Research Institute.
Many #bioinformatics jobs require a strong background in biology and/or computer science. Consider taking courses or gaining experience in these fields to enhance your career prospects.
Finally, don't be afraid to ask for help and advice from more experienced #bioinformaticians. Join online #communities and forums, such as our own, to connect with others and learn from their experiences.
We hope these tips have been helpful for getting started in bioinformatics. Join our #community to connect with other professionals and continue learning and growing in the field. Happy learning!
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#Genomic data provides information about the entire genetic makeup of a #biological system, including the #sequences of all its genes and the #regulation of their e#xpression.
Thread explaining a complete pipeline for #RNA-seq analysis 🧵
RNA-seq is a powerful technique that allows researchers to study the expression of genes at a global level. The RNA-seq analysis pipeline typically involves several different steps, including:
1. Quality control and filtering of the raw RNA-seq data 2. Alignment of the reads to the reference genome 3. Assembly of the aligned reads into transcripts 4. Quantification of gene and transcript expression levels