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DNA sequence analyzer

Analysis of a DNA sequence: base composition, GC content, complement and reverse complement, with ambiguous IUPAC codes supported.

Parameters

The sequence

Raw or FASTA sequence. Whitespace, line breaks and position numbering are ignored.

Composition along the sequence

301 bases · 25-base window
1000 %25 %50 %75 %100 %position (base)GCcenter at base 289overall GC 49.8 %max 92 % · base 13min 8 % · base 115GC 48 %

GC content of the windowuncertainty from ambiguous basesGC content of the whole sequencethe current window, on the sequence

centered on base 289

Playback varies only the window position, from one end of the sequence to the other in about twelve seconds, and every frame is fully recalculated.

GC content
(G + C) / N = 150 / 301 = 49.8339%
Window
25 bases, odd, slid along the whole sequence · 139 points plotted
Composition
301 determined bases, none ambiguous
Notes (2)

The y-axis runs from 0 to 100%, with no rescaling.

Profile smoothed over a sliding window of 25 bases: a departure from the overall GC content marks a locally GC-rich or AT-rich region.

Composition
A8427.9 %
T6722.3 %
G7424.6 %
C7625.2 %

Result

continuous calculation
GC content
GC49.8339%301 bases
Total length
301 bases
Determined bases
301
Both strands
Normalized sequence301 basesGCCGGCACGCCGGCGCACGGCCGCGGACGCCGGCGCAGGCCGGCACGCCGGCGCACGGCCGCGGACGCCGGCGCAGGCCGGCACGCCGGCGCACGGCCGCGATTATAAATTGATAATTTACATTAAATAGTTATTAAACATTTAAGATTATAAATTGATAATTTACATTAAATAGTTATTAAACATTTAAGATTATAAATTACGTTGACCATGCAGTACGATCCAGTTGCAATCGGATCACGTAGCTTGCAATGCCAGTTACGGATCAAGCTTGACCATGCAGTACGATCCAGTTGCAATC
Complement301 basesCGGCCGTGCGGCCGCGTGCCGGCGCCTGCGGCCGCGTCCGGCCGTGCGGCCGCGTGCCGGCGCCTGCGGCCGCGTCCGGCCGTGCGGCCGCGTGCCGGCGCTAATATTTAACTATTAAATGTAATTTATCAATAATTTGTAAATTCTAATATTTAACTATTAAATGTAATTTATCAATAATTTGTAAATTCTAATATTTAATGCAACTGGTACGTCATGCTAGGTCAACGTTAGCCTAGTGCATCGAACGTTACGGTCAATGCCTAGTTCGAACTGGTACGTCATGCTAGGTCAACGTTAG
Reverse complement301 basesGATTGCAACTGGATCGTACTGCATGGTCAAGCTTGATCCGTAACTGGCATTGCAAGCTACGTGATCCGATTGCAACTGGATCGTACTGCATGGTCAACGTAATTTATAATCTTAAATGTTTAATAACTATTTAATGTAAATTATCAATTTATAATCTTAAATGTTTAATAACTATTTAATGTAAATTATCAATTTATAATCGCGGCCGTGCGCCGGCGTGCCGGCCTGCGCCGGCGTCCGCGGCCGTGCGCCGGCGTGCCGGCCTGCGCCGGCGTCCGCGGCCGTGCGCCGGCGTGCCGGC

Calculation, assumptions and sources

OverviewBase composition, GC content, complement and reverse complement of a DNA sequence pasted as FASTA or raw text, with or without numbering.

Base composition, GC content, complement and reverse complement of a DNA sequence pasted as FASTA or raw text, with or without numbering. Invalid characters are flagged; IUPAC ambiguity codes are handled.

Method & formulasA ↔ T
A ↔ TG ↔ C

In double-stranded DNA, adenine (A) pairs with thymine (T) and guanine (G) with cytosine (C) (Watson-Crick rule). Ambiguous IUPAC codes follow the same rule: the complement of R (A or G) is Y (C or T).

R
purine, A or G.
Y
pyrimidine, C or T.
S
strong, 3 hydrogen bonds, G or C.
W
weak, 2 hydrogen bonds, A or T.
K
keto, G or T.
M
amino, A or C.
B, D, H, V
any base except A, C, G or T respectively.
N
any base, A, C, G or T.
Validity domainAn ambiguous code that may stand for either G/C or A/T (R, N…) gives a GC content as a range; S (G or C) and W (A or T) keep it exact.

An ambiguous code that may stand for either G/C or A/T (R, N…) gives a GC content as a range; S (G or C) and W (A or T) keep it exact. A sequence’s stability and melting temperature also depend on length, base order (stacking), ionic strength and concentration.

GC content: definitionGC content is the proportion of guanine (G) and cytosine (C) in the sequence, as a percentage.

GC content is the proportion of guanine (G) and cytosine (C) in the sequence, as a percentage. It varies between organisms and genome regions. G-C pairs, with 3 hydrogen bonds, are more thermally stable than A-T pairs, with 2.

Complement and reverse complementThe complement replaces each base with its complementary base.

The complement replaces each base with its complementary base. The reverse complement reads it backwards: it is the paired strand, read in its own 5'→3' direction (the strands are antiparallel), used to design a primer on the opposite strand.

EcoRI restriction siteGAATTC is the recognition site of the restriction enzyme EcoRI.

GAATTC is the recognition site of the restriction enzyme EcoRI. It is a palindrome: its reverse complement is the sequence itself, as for most sites of type II restriction enzymes.