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GPTomics

bio-sam-bam-basics

by GPTomics

a set of SKILLS.md for doing bioinformatics with agents like claude code

65🍴 17📅 2026年1月24日
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name: bio-sam-bam-basics description: View, convert, and understand SAM/BAM/CRAM alignment files using samtools and pysam. Use when inspecting alignments, converting between formats, or understanding alignment file structure. tool_type: cli primary_tool: samtools

SAM/BAM/CRAM Basics

View and convert alignment files using samtools and pysam.

Format Overview

FormatDescriptionUse Case
SAMText format, human-readableDebugging, small files
BAMBinary compressed SAMStandard storage format
CRAMReference-based compressionLong-term archival, smaller than BAM

SAM Format Structure

@HD VN:1.6 SO:coordinate
@SQ SN:chr1 LN:248956422
@RG ID:sample1 SM:sample1
@PG ID:bwa PN:bwa VN:0.7.17
read1  0   chr1  100  60  50M  *  0  0  ACGT...  FFFF...  NM:i:0

Header lines start with @:

  • @HD - Header metadata (version, sort order)
  • @SQ - Reference sequence dictionary
  • @RG - Read group information
  • @PG - Program used to create file

Alignment fields (tab-separated):

  1. QNAME - Read name
  2. FLAG - Bitwise flag
  3. RNAME - Reference name
  4. POS - 1-based position
  5. MAPQ - Mapping quality
  6. CIGAR - Alignment description
  7. RNEXT - Mate reference
  8. PNEXT - Mate position
  9. TLEN - Template length
  10. SEQ - Read sequence
  11. QUAL - Base qualities
  12. Optional tags (NM:i:0, MD:Z:50, etc.)

samtools view

View BAM as SAM

samtools view input.bam | head

View with Header

samtools view -h input.bam | head -100

View Header Only

samtools view -H input.bam

View Specific Region

samtools view input.bam chr1:1000-2000

Count Alignments

samtools view -c input.bam

Format Conversion

BAM to SAM

samtools view -h -o output.sam input.bam

SAM to BAM

samtools view -b -o output.bam input.sam

BAM to CRAM

samtools view -C -T reference.fa -o output.cram input.bam

CRAM to BAM

samtools view -b -T reference.fa -o output.bam input.cram

Pipe Conversion

samtools view -b input.sam > output.bam

Common Flags

FlagDecimalMeaning
0x11Paired
0x22Proper pair
0x44Unmapped
0x88Mate unmapped
0x1016Reverse strand
0x2032Mate reverse strand
0x4064First in pair
0x80128Second in pair
0x100256Secondary alignment
0x200512Failed QC
0x4001024PCR duplicate
0x8002048Supplementary

Decode Flags

samtools flags 147
# 0x93 147 PAIRED,PROPER_PAIR,REVERSE,READ2

CIGAR Operations

OpDescription
MAlignment match (can be mismatch)
IInsertion to reference
DDeletion from reference
NSkipped region (introns in RNA-seq)
SSoft clipping
HHard clipping
=Sequence match
XSequence mismatch

Example: 50M2I30M = 50 bases match, 2 base insertion, 30 bases match

pysam Python Alternative

Open and Iterate

import pysam

with pysam.AlignmentFile('input.bam', 'rb') as bam:
    for read in bam:
        print(f'{read.query_name}\t{read.reference_name}:{read.reference_start}')

Access Header

with pysam.AlignmentFile('input.bam', 'rb') as bam:
    for sq in bam.header['SQ']:
        print(f'{sq["SN"]}: {sq["LN"]} bp')

Read Alignment Properties

with pysam.AlignmentFile('input.bam', 'rb') as bam:
    for read in bam:
        print(f'Name: {read.query_name}')
        print(f'Flag: {read.flag}')
        print(f'Chrom: {read.reference_name}')
        print(f'Pos: {read.reference_start}')  # 0-based
        print(f'MAPQ: {read.mapping_quality}')
        print(f'CIGAR: {read.cigarstring}')
        print(f'Seq: {read.query_sequence}')
        print(f'Qual: {read.query_qualities}')
        break

Check Flag Properties

with pysam.AlignmentFile('input.bam', 'rb') as bam:
    for read in bam:
        if read.is_paired and read.is_proper_pair:
            if read.is_reverse:
                strand = '-'
            else:
                strand = '+'
            print(f'{read.query_name} on {strand} strand')

Fetch Region

with pysam.AlignmentFile('input.bam', 'rb') as bam:
    for read in bam.fetch('chr1', 1000, 2000):
        print(read.query_name)

Convert BAM to SAM

with pysam.AlignmentFile('input.bam', 'rb') as infile:
    with pysam.AlignmentFile('output.sam', 'w', header=infile.header) as outfile:
        for read in infile:
            outfile.write(read)

Convert to CRAM

with pysam.AlignmentFile('input.bam', 'rb') as infile:
    with pysam.AlignmentFile('output.cram', 'wc', reference_filename='reference.fa', header=infile.header) as outfile:
        for read in infile:
            outfile.write(read)

Quick Reference

Tasksamtoolspysam
View BAMsamtools view file.bamAlignmentFile('file.bam', 'rb')
View headersamtools view -H file.bambam.header
Count readssamtools view -c file.bamsum(1 for _ in bam)
Get regionsamtools view file.bam chr1:1-1000bam.fetch('chr1', 0, 1000)
BAM to SAMsamtools view -h -o out.sam in.bamOpen with 'w' mode
SAM to BAMsamtools view -b -o out.bam in.samOpen with 'wb' mode
BAM to CRAMsamtools view -C -T ref.fa -o out.cram in.bamOpen with 'wc' mode
  • alignment-indexing - Create indices for random access (required for fetch/region queries)
  • alignment-sorting - Sort alignments by coordinate or name
  • alignment-filtering - Filter alignments by flags, quality, regions
  • alignment-statistics - Generate statistics from alignment files
  • sequence-io/read-sequences - Parse FASTA/FASTQ input files

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